Cleared Special

K063590 - V.A.C. FREEDOM CANISTER, MODEL M6275421 (FDA 510(k) Clearance)

Also includes:
V.A.C. ATS CANISTER, MODELS K6275422, M6275423
Jan 2007
Decision
55d
Days
Class 2
Risk

K063590 is an FDA 510(k) clearance for the V.A.C. FREEDOM CANISTER, MODEL M6275421. This device is classified as a Negative Pressure Wound Therapy Powered Suction Pump (Class II - Special Controls, product code OMP).

Submitted by Kci USA, Inc. (San Antonio, US). The FDA issued a Cleared decision on January 25, 2007, 55 days after receiving the submission on December 1, 2006.

This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4780. For Wound Management Via Application Of Continual Or Intermittent Negative Pressure To The Wound For Removal Of Fluids, Including Wound Exudate, Irrigation Fluids, And Infectious Materials. The Device Is Indicated For Management Of Chronic, Acute, Traumatic, Subacute And Dehisced Wounds, Partial-thickness Burns, Ulcers (such As Diabetic Or Pressure), Flaps And Grafts..

Submission Details

510(k) Number K063590 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 01, 2006
Decision Date January 25, 2007
Days to Decision 55 days
Submission Type Special
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code OMP — Negative Pressure Wound Therapy Powered Suction Pump
Device Class Class II - Special Controls
CFR Regulation 21 CFR 878.4780
Definition For Wound Management Via Application Of Continual Or Intermittent Negative Pressure To The Wound For Removal Of Fluids, Including Wound Exudate, Irrigation Fluids, And Infectious Materials. The Device Is Indicated For Management Of Chronic, Acute, Traumatic, Subacute And Dehisced Wounds, Partial-thickness Burns, Ulcers (such As Diabetic Or Pressure), Flaps And Grafts.

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