ALLCLENZ WOUND CLEANSER— 510(k) K965120

Name: FDA 510(k) clearance K965120
Creator: U.S. Food and Drug Administration
Published: 1997-03-21

Substantially Equivalent for Some Indications

Dpt Laboratories, Ltd.

FDA 510(k) clearance K965120 for ALLCLENZ WOUND CLEANSER, Substantially Equivalent for Some Indications on 1997-03-21. Applicant: Dpt Laboratories, Ltd.. Device class: 1.

Clearance details

Applicant: Dpt Laboratories, Ltd.
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 1996-12-23
Decision date: 1997-03-21
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Fort Worth, TX, US

Download summary PDF View on FDA.gov ↗

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