Cleared Traditional

INJECT-SNARE (K942110) - FDA 510(k) Clearance

Class II Gastroenterology & Urology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K942110 · Endovations · Gastroenterology & Urology device
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Oct 1994
Decision
164d
Days
Class 2
Risk

K942110 is an FDA 510(k) clearance for the INJECT-SNARE. Classified as Snare, Flexible (product code FDI), Class II - Special Controls.

Submitted by Endovations (Reading, US). The FDA issued a Cleared decision on October 13, 1994 after a review of 164 days - an extended review cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.4300 - 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 Endovations devices

Submission Details

510(k) Number K942110 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 02, 1994
Decision Date October 13, 1994
Days to Decision 164 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
34d slower than avg
Panel avg: 130d · This submission: 164d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code FDI Snare, Flexible
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.4300
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 Peers - FDI Snare, Flexible

All 25
Devices cleared under the same product code (FDI) and FDA review panel - the closest regulatory comparables to K942110.
SENSATION SHORT THROW, CAPTIFLEX, CAPTIVATOR, CAPTIVATOR II, PROFILE, SINGLE-USE POLYPECTOMY SNARES
K131700 · Boston Scientific Corp · Nov 2013
SNARE, FLEXIBLE, ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESSORIES
K950496 · Boston Scientific Corp · Mar 1995
PROPOSED TRADEMAN MICROVASIVE POLYPECTOMY SNARES
K941750 · Boston Scientific Corp · Nov 1994
SPHINCTEROTOME
K930022 · Boston Scientific Corp · Apr 1993
DAVOL POLYPECTOMY SNARE
K845016 · C.R. Bard, Inc. · Jan 1985