Cleared Traditional

K902107 - WILSON-COOK SYRINGE HOLDERS

K902107 is the FDA 510(k) clearance for WILSON-COOK SYRINGE HOLDERS by Wilson-Cook Medical, Inc.. It is a Class 2 Gastroenterology & Urology device (product code FGE) cleared through the Traditional 510(k) pathway after a 69-day FDA review.

K902107 · Wilson-Cook Medical, Inc. · Gastroenterology & Urology device
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Jul 1990
Decision
69d
Days
Class 2
Risk

K902107 is an FDA 510(k) clearance for the WILSON-COOK SYRINGE HOLDERS. Classified as Stents, Drains And Dilators For The Biliary Ducts (product code FGE), Class II - Special Controls.

Submitted by Wilson-Cook Medical, Inc. (Winston-Salem, US). The FDA issued a Cleared decision on July 16, 1990 after a review of 69 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5010 - 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 Wilson-Cook Medical, Inc. devices

Submission Details

510(k) Number K902107 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 08, 1990
Decision Date July 16, 1990
Days to Decision 69 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
61d faster than avg
Panel avg: 130d · This submission: 69d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code FGE Stents, Drains And Dilators For The Biliary Ducts
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5010
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 - FGE Stents, Drains And Dilators For The Biliary Ducts

All 300
Devices cleared under the same product code (FGE) and FDA review panel - the closest regulatory comparables to K902107.
SOEHENDRA STENT RETRIEVER
K903420 · Wilson-Cook Medical, Inc. · Oct 1990
COOK-GIANTURCO ROSCH BILIARY Z-STENT, MODIFICATION
K903858 · Cook, Inc. · Oct 1990
PR CANNULAS
K902734 · Olympus Corp. · Aug 1990
DOBBHOFF BILIARY STENT SET
K901582 · Biosearch Medical Products, Inc. · Jun 1990
CANDELA DIRECTABLE BILIARY CATHETER SYSTEM
K900904 · Candela Laser Corp. · May 1990
WILSON-COOK ENDOSCOPIC NASAL BILIARY DRAINAGE SETS
K896323 · Wilson-Cook Medical, Inc. · Apr 1990