WMI DVT WRAP, WMI THERMAL WRAP MODEL: D-1000F, D-1000C, T-2000A, T-2000B, T-2000KF, T-2000S, T-2000N— 510(k) K100969

Name: FDA 510(k) clearance K100969
Creator: U.S. Food and Drug Administration
Published: 2010-09-20

Substantially Equivalent

Wmi Enterprises, LLC

FDA 510(k) clearance K100969 for WMI DVT WRAP, WMI THERMAL WRAP MODEL: D-1000F, D-1000C, T-2000A, T-2000B, T-2000KF, T-2000S, T-2000N, Substantially Equivalent on 2010-09-20. Applicant: Wmi Enterprises, LLC. Device class: 2.

Clearance details

Applicant: Wmi Enterprises, LLC
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2010-04-08
Decision date: 2010-09-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicago, IL, US

Download summary PDF View on FDA.gov ↗

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