VASOPRESS SUPREME MINI MODEL VP500DM— 510(k) K101915

Name: FDA 510(k) clearance K101915
Creator: U.S. Food and Drug Administration
Published: 2010-08-06

Substantially Equivalent

Compression Therapy Concepts, Inc.

FDA 510(k) clearance K101915 for VASOPRESS SUPREME MINI MODEL VP500DM, Substantially Equivalent on 2010-08-06. Applicant: Compression Therapy Concepts, Inc.. Device class: 2.

Clearance details

Applicant: Compression Therapy Concepts, Inc.
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2010-07-09
Decision date: 2010-08-06
Decision: Substantially Equivalent
Clearance type: Special
Location: Eatontown, NJ, US

Download summary PDF View on FDA.gov ↗

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