LYMPHA PRESS PLUS DEVICE— 510(k) K013331

Substantially Equivalent

Mego Afek

FDA 510(k) clearance K013331 for LYMPHA PRESS PLUS DEVICE, Substantially Equivalent on 2001-11-30. Applicant: Mego Afek.

Clearance details

Applicant: Mego Afek
Product code: Code JOW
Advisory panel: Cardiovascular
Date received: 2001-10-05
Decision date: 2001-11-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kfar Saba, IL

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