UUHC REPROCESSED COMPRESSION SLEEVE DEVICES— 510(k) K031189

Name: FDA 510(k) clearance K031189
Creator: U.S. Food and Drug Administration
Published: 2003-10-16

Substantially Equivalent

University of Utah Hospitals and Clinics

FDA 510(k) clearance K031189 for UUHC REPROCESSED COMPRESSION SLEEVE DEVICES, Substantially Equivalent on 2003-10-16. Applicant: University of Utah Hospitals and Clinics. Device class: 2.

Clearance details

Applicant: University of Utah Hospitals and Clinics
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2003-04-15
Decision date: 2003-10-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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