STERIKING, SEE & PEEL— 510(k) K922440

Name: FDA 510(k) clearance K922440
Creator: U.S. Food and Drug Administration
Published: 1994-09-26

Substantially Equivalent

Cox Sterile Products, Inc.

FDA 510(k) clearance K922440 for STERIKING, SEE & PEEL, Substantially Equivalent on 1994-09-26. Applicant: Cox Sterile Products, Inc.. Device class: 2.

Clearance details

Applicant: Cox Sterile Products, Inc.
Product code: Code KCT
Device class: Class 2
Regulation: 21 CFR 880.6850
Advisory panel: General Hospital
Date received: 1992-05-22
Decision date: 1994-09-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dallas, TX, US

Download summary PDF View on FDA.gov ↗

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