K896383 is an FDA 510(k) clearance for the DISPOSABLE EXTERNAL CLAMPS. Classified as Dissector, Surgical, General & Plastic Surgery (product code GDI), Class I - General Controls.
Submitted by Galenica Enterprises, Inc. (Quebec Canada J7e 4h7, CA). The FDA issued a Cleared decision on December 6, 1989 after a review of 30 days - a notably fast clearance cycle.
This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4800 - the FDA general and plastic surgery device framework. 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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