ARTERIOFLOW MODEL 7500 SEQUENTIAL COMPRESSION DEVICE— 510(k) K102582

Substantially Equivalent

Devon Medical, Inc.

FDA 510(k) clearance K102582 for ARTERIOFLOW MODEL 7500 SEQUENTIAL COMPRESSION DEVICE, Substantially Equivalent on 2010-10-07. Applicant: Devon Medical, Inc..

Clearance details

Applicant: Devon Medical, Inc.
Product code: Code JOW
Advisory panel: Cardiovascular
Date received: 2010-09-08
Decision date: 2010-10-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: King Of Prussia, PA, US

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