SURGICAL PREP RAZOR, STRAIGHT TYPE— 510(k) K874234

Name: FDA 510(k) clearance K874234
Creator: U.S. Food and Drug Administration
Published: 1987-11-02

Substantially Equivalent

Derma-Safe Co.

FDA 510(k) clearance K874234 for SURGICAL PREP RAZOR, STRAIGHT TYPE, Substantially Equivalent on 1987-11-02. Applicant: Derma-Safe Co.. Device class: 1.

Clearance details

Applicant: Derma-Safe Co.
Product code: Code LWK
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1987-10-15
Decision date: 1987-11-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wayne, NJ, US

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Recent devices under product code LWK

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K946162 — 3M(TM) SURGICAL SLIPPER, 9660 SERIES1995-01-24
K910524 — SURGICAL CLIPPER1991-03-28
K874370 — SURGICAL PREP RAZOR1987-11-13

Data sourced from openFDA. This site is unofficial and independent of the FDA.