Cleared Traditional

NON-ADHERENT PAD (K852412) - FDA 510(k) Clearance

K852412 · American White Cross, Inc. · General & Plastic Surgery device
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Jul 1985
Decision
53d
Days
-
Risk

K852412 is an FDA 510(k) clearance for the NON-ADHERENT PAD. Classified as Gauze/sponge, Internal (product code EFQ).

Submitted by American White Cross, Inc. (Stamford, US). The FDA issued a Cleared decision on July 29, 1985 after a review of 53 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 American White Cross, Inc. devices

Submission Details

510(k) Number K852412 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 06, 1985
Decision Date July 29, 1985
Days to Decision 53 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
62d faster than avg
Panel avg: 115d · This submission: 53d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code EFQ Gauze/sponge, Internal
Device Class -