Cleared Traditional

K931933 - CHAD LABS ADHESIVE BANDAGE REMOVER
(FDA 510(k) Clearance)

K931933 · Chad Labs Corp. · General & Plastic Surgery
Jul 1993
Decision
80d
Days
Class 1
Risk

K931933 is an FDA 510(k) clearance for the CHAD LABS ADHESIVE BANDAGE REMOVER, a Solvent, Adhesive Tape (Class I — General Controls, product code KOX), submitted by Chad Labs Corp. (Milford, US). The FDA issued a Cleared decision on July 8, 1993, 80 days after receiving the submission on April 19, 1993. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4730.

Submission Details

510(k) Number K931933 FDA.gov
FDA Decision Cleared SESE
Date Received April 19, 1993
Decision Date July 08, 1993
Days to Decision 80 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement

Device Classification

Product Code KOX — Solvent, Adhesive Tape
Device Class Class I — General Controls
CFR Regulation 21 CFR 878.4730

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