Cleared Traditional

K992817 - ANTIBACTERIAL ADHESIVE BANDAGE

K992817 · William Feinstein & Associates, Inc. · General & Plastic Surgery device
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Nov 1999
Decision
77d
Days
-
Risk

K992817 is an FDA 510(k) clearance for the ANTIBACTERIAL ADHESIVE BANDAGE. Classified as Dressing, Wound, Drug (product code FRO).

Submitted by William Feinstein & Associates, Inc. (New York, US). The FDA issued a Cleared decision on November 5, 1999 after a review of 77 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 William Feinstein & Associates, Inc. devices

FDA 510(k) Submission Details - K992817

510(k) Number K992817 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 20, 1999
Decision Date November 05, 1999
Days to Decision 77 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
38d faster than avg
Panel avg: 115d · This submission: 77d
Pathway characteristics
Predicate-based equivalence.

FRO Device Classification - Class 0,

Product Code FRO Dressing, Wound, Drug
Device Class -

Regulatory Peers - FRO Dressing, Wound, Drug

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