PHLEBOPRESS MODEL 601A COMPRESSION THERAPY DEVICE— 510(k) K072372

Name: FDA 510(k) clearance K072372
Creator: U.S. Food and Drug Administration
Published: 2007-11-21

Substantially Equivalent

Mego Afek

FDA 510(k) clearance K072372 for PHLEBOPRESS MODEL 601A COMPRESSION THERAPY DEVICE, Substantially Equivalent on 2007-11-21. Applicant: Mego Afek. Device class: 2.

Clearance details

Applicant: Mego Afek
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2007-08-23
Decision date: 2007-11-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kfar Saba, IL

Download summary PDF View on FDA.gov ↗

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