Cleared Traditional

K862126 - STERILE LAPAROTOMY GAUZE SPONGE (FDA 510(k) Clearance)

K862126 · Anago, Inc. · General & Plastic Surgery device
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Jun 1986
Decision
15d
Days
-
Risk

K862126 is an FDA 510(k) clearance for the STERILE LAPAROTOMY GAUZE SPONGE. Classified as Gauze/sponge, Internal (product code EFQ).

Submitted by Anago, Inc. (Fort Worth, US). The FDA issued a Cleared decision on June 19, 1986 after a review of 15 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 Anago, Inc. devices

Submission Details

510(k) Number K862126 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 04, 1986
Decision Date June 19, 1986
Days to Decision 15 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
99d faster than avg
Panel avg: 114d · This submission: 15d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code EFQ Gauze/sponge, Internal
Device Class -