LYMPHA PRESS OPTIMAL, MODEL# 1201AP— 510(k) K082149

Name: FDA 510(k) clearance K082149
Creator: U.S. Food and Drug Administration
Published: 2008-10-06

Substantially Equivalent

Mego Afek AC , Ltd.

FDA 510(k) clearance K082149 for LYMPHA PRESS OPTIMAL, MODEL# 1201AP, Substantially Equivalent on 2008-10-06. 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: 2008-07-30
Decision date: 2008-10-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kfar Saba, IL

Download summary PDF View on FDA.gov ↗

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