ACTIVECARE DVT, ACTIVECARE+SFT, AND ACTIVECARE+DTX SYSTEMS— 510(k) K140755

Name: FDA 510(k) clearance K140755
Creator: U.S. Food and Drug Administration
Published: 2014-05-08

Substantially Equivalent

Medical Compression Systems (Dbn) , Ltd.

FDA 510(k) clearance K140755 for ACTIVECARE DVT, ACTIVECARE+SFT, AND ACTIVECARE+DTX SYSTEMS, Substantially Equivalent on 2014-05-08. Applicant: Medical Compression Systems (Dbn) , Ltd.. Device class: 2.

Clearance details

Applicant: Medical Compression Systems (Dbn) , Ltd.
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2014-03-26
Decision date: 2014-05-08
Decision: Substantially Equivalent
Clearance type: Special
Location: Or-Akiva, IL

Download summary PDF View on FDA.gov ↗

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More clearances from Medical Compression Systems (Dbn) , Ltd.

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K160431 — ActiveCare Home2016-07-13
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K110159 — ACTIVECARE SFT2011-05-12
K060146 — ACTIVECARE ++ SYSTEM2006-03-08
K023573 — WIZAIR COMPRESSION SYSTEM2002-11-21

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