JSA REPROCESSED COMPRESSION SLEEVE DEVICES— 510(k) K031722

Name: FDA 510(k) clearance K031722
Creator: U.S. Food and Drug Administration
Published: 2003-11-25

Substantially Equivalent

Jack Speer and Assoc., Inc.

FDA 510(k) clearance K031722 for JSA REPROCESSED COMPRESSION SLEEVE DEVICES, Substantially Equivalent on 2003-11-25. Applicant: Jack Speer and Assoc., Inc.. Device class: 2.

Clearance details

Applicant: Jack Speer and Assoc., Inc.
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2003-06-03
Decision date: 2003-11-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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