K860486 - ACTISORB ACTIVATED CHARCOAL DRESSING (FDA 510(k) Clearance)

K860486 is an FDA 510(k) clearance for the ACTISORB ACTIVATED CHARCOAL DRESSING. Classified as Dressing, Wound, Drug (product code FRO).

Submitted by Johnson & Johnson Professionals, Inc. (Raynham, US). The FDA issued a Cleared decision on March 26, 1986 after a review of 44 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.

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