Cleared Traditional

K871002 - 1X5YD

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Mar 1987
Decision
20d
Days
-
Risk

K871002 is an FDA 510(k) clearance for the 1X5YD,2X6YD,3X5YD,4X6YD,1/2/3X10YD GAUZE. Classified as Gauze/sponge, Internal (product code EFQ).

Submitted by Advantage Credit Services, Inc. (Kansas City, US). The FDA issued a Cleared decision on March 31, 1987 after a review of 20 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel. 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 Advantage Credit Services, Inc. devices

Submission Details

510(k) Number K871002 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 11, 1987
Decision Date March 31, 1987
Days to Decision 20 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
95d faster than avg
Panel avg: 115d · This submission: 20d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code EFQ Gauze/sponge, Internal
Device Class -

Regulatory Peers - EFQ Gauze/sponge, Internal

All 39
Devices cleared under the same product code (EFQ) and FDA review panel - the closest regulatory comparables to K871002.
ENVINET(TM)
K874551 · Marion Laboratories, Inc. · Jan 1988
PHARMANET (TM)
K872572 · Pharmacia, Inc. · Jan 1988
AQUATULLE FINE MESH NON-ADHERING DRESSING
K872759 · Smith & Nephew, Inc. · Sep 1987
STERILE LAPAROTOMY GAUZE SPONGE
K862126 · Anago, Inc. · Jun 1986
NU-GAUZE SPONGE
K821150 · Johnson & Johnson Professionals, Inc. · Aug 1982
SOFTCARE BARRIER WET DRESSING
K812736 · The Kendal Co. · Nov 1981