Cleared Traditional

ACELL UBM HYDRATED WOUND DRESSING

K022854 · Acell, Inc. · General & Plastic Surgery
Dec 2002
Decision
137d
Days
Risk

About This 510(k) Submission

K022854 is an FDA 510(k) clearance for the ACELL UBM HYDRATED WOUND DRESSING, a Wound Dressing With Animal-derived Material(s), submitted by Acell, Inc. (Washington, US). The FDA issued a Cleared decision on December 30, 2002, 137 days after receiving the submission on August 15, 2002. This device falls under the General & Plastic Surgery review panel.

Submission Details

510(k) Number K022854 FDA.gov
FDA Decision Cleared SESE
Date Received August 15, 2002
Decision Date December 30, 2002
Days to Decision 137 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code KGN — Wound Dressing With Animal-derived Material(s)
Device Class