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. 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: 2001-10-05
Decision date: 2001-11-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kfar Saba, IL

Download summary PDF View on FDA.gov ↗

Recent devices under product code JOW

K261807 — Sequential Circulator (SC-4004-DL, SC-4008-DL)2026-09-11
K254217 — Aerloom2026-08-31
K253555 — Flexitouch® Plus Advanced Pneumatic Compression System2026-07-31
K253386 — DVT Garment2026-06-25
K250242 — Compression Therapy Device (LGT-2202DVT)2026-04-24

More clearances from Mego Afek

K230385 — Ballancer Platinum (1222)2023-04-04
K072372 — PHLEBOPRESS MODEL 601A COMPRESSION THERAPY DEVICE2007-11-21
K060220 — PBS MODEL 701A COMPRESSION THERAPY DEVICE2006-02-09
K810338 — LYMPHA PRESS1981-10-20

Data sourced from openFDA. This site is unofficial and independent of the FDA.