PRACTICAL COMPRESSION DEVICE (PCD) 901A&901B— 510(k) K121962

Name: FDA 510(k) clearance K121962
Creator: U.S. Food and Drug Administration
Published: 2012-10-19

Substantially Equivalent

Mego Afek AC , Ltd.

FDA 510(k) clearance K121962 for PRACTICAL COMPRESSION DEVICE (PCD) 901A&901B, Substantially Equivalent on 2012-10-19. Applicant: Mego Afek AC , Ltd.. Device class: 2.

Clearance details

Applicant: Mego Afek AC , Ltd.
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2012-07-05
Decision date: 2012-10-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Afek, IL

Download summary PDF View on FDA.gov ↗

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