Cleared Traditional

K051082 - MEDTRADE PRODUCTS SKIN PROTECTIVE BARRIER WIPE (STERILE AND PRESERVED) (FDA 510(k) Clearance)

Nov 2005
Decision
195d
Days
Class 1
Risk

K051082 is an FDA 510(k) clearance for the MEDTRADE PRODUCTS SKIN PROTECTIVE BARRIER WIPE (STERILE AND PRESERVED). This device is classified as a Bandage, Liquid (Class I - General Controls, product code KMF).

Submitted by Medtrade Products , Ltd. (Crewe, GB). The FDA issued a Cleared decision on November 8, 2005, 195 days after receiving the submission on April 27, 2005.

This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 880.5090.

Submission Details

510(k) Number K051082 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 27, 2005
Decision Date November 08, 2005
Days to Decision 195 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code KMF — Bandage, Liquid
Device Class Class I - General Controls
CFR Regulation 21 CFR 880.5090