JOYKEY SURGICAL DRAPES (STERILE)— 510(k) K062480

Name: FDA 510(k) clearance K062480
Creator: U.S. Food and Drug Administration
Published: 2007-03-05

Substantially Equivalent

Joykey Industryial , Ltd.

FDA 510(k) clearance K062480 for JOYKEY SURGICAL DRAPES (STERILE), Substantially Equivalent on 2007-03-05. Applicant: Joykey Industryial , Ltd.. Device class: 2.

Clearance details

Applicant: Joykey Industryial , Ltd.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 2006-08-24
Decision date: 2007-03-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Flagstaff, AZ, US

Download summary PDF View on FDA.gov ↗

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