Cleared Traditional

K132340 - ERBEFLO CLEVERCAP HYBRID TUBING/CAP SET...

K132340 is the FDA 510(k) clearance for ERBEFLO CLEVERCAP HYBRID TUBING/CAP SET... by Erbe USA, Inc.. It is a Class 2 Gastroenterology & Urology device (product code FEQ) cleared through the Traditional 510(k) pathway after a 144-day FDA review.

K132340 · Erbe USA, Inc. · Gastroenterology & Urology device
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Dec 2013
Decision
144d
Days
Class 2
Risk

K132340 is an FDA 510(k) clearance for the ERBEFLO CLEVERCAP HYBRID TUBING/CAP SET FOR PENTAX SCOPES, ERBEFLO CLEVERCAP .... Classified as Pump, Air, Non-manual, For Endoscope (product code FEQ), Class II - Special Controls.

Submitted by Erbe USA, Inc. (Marietta, US). The FDA issued a Cleared decision on December 17, 2013 after a review of 144 days - within the typical 510(k) review window.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.1500 - the FDA gastroenterology and urology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Gastroenterology & Urology review framework, consistent with the majority of Class II 510(k) submissions.

View all Erbe USA, Inc. devices

Submission Details

510(k) Number K132340 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 26, 2013
Decision Date December 17, 2013
Days to Decision 144 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review Yes - reviewed by an FDA-accredited third party
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
14d slower than avg
Panel avg: 130d · This submission: 144d
Pathway characteristics
Predicate-based equivalence. No clinical trials required. Third-party reviewed.

Device Classification

Product Code FEQ Pump, Air, Non-manual, For Endoscope
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.1500
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Gastroenterology & Urology devices follow this clearance model.

Regulatory Consultant

Regulatory Technology Services, LLC

The regulatory consultant manages the 510(k) submission process on behalf of the applicant - coordinating technical documentation, predicate strategy and FDA communications. Identifying the consultant behind a submission is a key signal for competitive regulatory intelligence.

Regulatory Peers - FEQ Pump, Air, Non-manual, For Endoscope

All 9
Devices cleared under the same product code (FEQ) and FDA review panel - the closest regulatory comparables to K132340.
AquaShield System CO2- Fujifilm
K173650 · United States Endoscopy Group, Inc. · Jan 2018
Erbe’s CO2 Tubing/Cap Sets
K162152 · Erbe USA, Inc. · Aug 2016
AquaShield system CO2, AquaShield system-PENTAX
K153362 · United States Endoscopy Group, Inc. · Dec 2015
AQUASHIELD CO2 SYSTEM
K120123 · United States Endoscopy Group, Inc. · Mar 2012
ERBEFLO CLEVERCAP HYBRID TUBING/CAP SETS FOR OLYMPUS MODELS 160 AND 180 SERIES SCOPES
K103696 · Erbe USA, Inc. · Mar 2011
WATER BOTTLE CAP SYSTEM
K101146 · United States Endoscopy Group, Inc. · Jul 2010

Related FDA 510(k) Regulatory Insights

Additional regulatory intelligence related to this FDA 510(k) submission, including predicate strategy, review pathways and device classification guidance.