Cleared Traditional

AQUACEL AG FOAM HYDROFIBER FOAM DRESSING WITH SILVER, ADHESIVE AND NON ADHESIVE

K123481 · Convatec, Inc. · General & Plastic Surgery
Jun 2013
Decision
205d
Days
Risk

About This 510(k) Submission

K123481 is an FDA 510(k) clearance for the AQUACEL AG FOAM HYDROFIBER FOAM DRESSING WITH SILVER, ADHESIVE AND NON ADHESIVE, a Dressing, Wound, Drug, submitted by Convatec, Inc. (Skillman, US). The FDA issued a Cleared decision on June 6, 2013, 205 days after receiving the submission on November 13, 2012. This device falls under the General & Plastic Surgery review panel.

Submission Details

510(k) Number K123481 FDA.gov
FDA Decision Cleared SESE
Date Received November 13, 2012
Decision Date June 06, 2013
Days to Decision 205 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code FRO — Dressing, Wound, Drug
Device Class

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