Cleared Traditional

BIOBRANE BRAND TEMP. WOUND DRESSING W/ADHESIVE (K844052) - FDA 510(k) Clearance

K844052 · Woodroof Laboratories, Inc. · General & Plastic Surgery device
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Jan 1985
Decision
97d
Days
-
Risk

K844052 is an FDA 510(k) clearance for the BIOBRANE BRAND TEMP. WOUND DRESSING W/ADHESIVE.

Submitted by Woodroof Laboratories, Inc. (Santa Ana, US). The FDA issued a Cleared decision on January 23, 1985 after a review of 97 days - within the typical 510(k) review window.

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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

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Submission Details

510(k) Number K844052 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 18, 1984
Decision Date January 23, 1985
Days to Decision 97 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
18d faster than avg
Panel avg: 115d · This submission: 97d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -