Cleared Traditional

K855160 - CARE IV BURN PAD, CATALOG #'S BP2334,BP3472

K855160 · Howard Associates, Inc. · General & Plastic Surgery device
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Jan 1986
Decision
29d
Days
-
Risk

K855160 is an FDA 510(k) clearance for the CARE IV BURN PAD, CATALOG #'S BP2334,BP3472.

Submitted by Howard Associates, Inc. (Dallas, US). The FDA issued a Cleared decision on January 24, 1986 after a review of 29 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 Howard Associates, Inc. devices

FDA 510(k) Submission Details - K855160

510(k) Number K855160 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 26, 1985
Decision Date January 24, 1986
Days to Decision 29 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
86d faster than avg
Panel avg: 115d · This submission: 29d
Pathway characteristics
Predicate-based equivalence.

Device Classification - Class ,

Product Code -
Device Class -