VESOFLOW PLUS DVT COMPRESSION DEVICE— 510(k) K141064

Name: FDA 510(k) clearance K141064
Creator: U.S. Food and Drug Administration
Published: 2014-12-04

Substantially Equivalent

Caremed Supply, Inc.

FDA 510(k) clearance K141064 for VESOFLOW PLUS DVT COMPRESSION DEVICE, Substantially Equivalent on 2014-12-04. Applicant: Caremed Supply, Inc.. Device class: 2.

Clearance details

Applicant: Caremed Supply, Inc.
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2014-04-24
Decision date: 2014-12-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New Taipei City, TW

Download summary PDF View on FDA.gov ↗

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