JSA REPROCESSED COMPRESSION SLEEVE DEVICES— 510(k) K031722

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..

Clearance details

Applicant: Jack Speer and Assoc., Inc.
Product code: Code JOW
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 ↗

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