Cleared Traditional

K812685 - ERICKA NEG. PRESSURE ARTERIAL BLOOD LINE

K812685 is the FDA 510(k) clearance for ERICKA NEG. PRESSURE ARTERIAL BLOOD LINE by Ericka. It is a Class 2 Gastroenterology & Urology device (product code FJK) cleared through the Traditional 510(k) pathway after a 7-day FDA review.

K812685 · Ericka · Gastroenterology & Urology device
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Sep 1981
Decision
7d
Days
Class 2
Risk

K812685 is an FDA 510(k) clearance for the ERICKA NEG. PRESSURE ARTERIAL BLOOD LINE. Classified as Set, Tubing, Blood, With And Without Anti-regurgitation Valve (product code FJK), Class II - Special Controls.

Submitted by Ericka (Walker, US). The FDA issued a Cleared decision on September 29, 1981 after a review of 7 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5820 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Ericka devices

Submission Details

510(k) Number K812685 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 22, 1981
Decision Date September 29, 1981
Days to Decision 7 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
123d faster than avg
Panel avg: 130d · This submission: 7d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code FJK Set, Tubing, Blood, With And Without Anti-regurgitation Valve
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5820
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 - FJK Set, Tubing, Blood, With And Without Anti-regurgitation Valve

All 43
Devices cleared under the same product code (FJK) and FDA review panel - the closest regulatory comparables to K812685.
BLOOD LINE SETS FOR HEMOFILTRATION
K830677 · Gambro, Inc. · Apr 1983
TS-180 SERIES TUBING SET
K821138 · Extracorporeal Medical Specialities, Inc. · May 1982
MALE LUER CONNECTOR & HINGED CAP
K820169 · Extracorporeal Medical Specialities, Inc. · Feb 1982
ERIKA EXTENSION SETS
K810823 · Erika, Inc. · Apr 1981
ERIKA HEPARIN INFUSION ADAPTOR
K810824 · Erika, Inc. · Apr 1981
ARTERIOVENOUS BLOOD TUBING SETS
K802874 · Extracorporeal Medical Specialities, Inc. · Nov 1980