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FDA 510(k), K942530, ART-ASSIST MODEL AA-1000
FDA 510(k), K942530, ART-ASSIST MODEL AA-1000
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510(K) Number: K942530
Device Name: ART-ASSIST MODEL AA-1000
Manufacturer: ACI MEDICAL, INC.
Device Classification Name: sleeve, limb, compressible
Regulation Number: 870.5800
Classification Product Code: JOW
Date Received: 05/27/1994
Decision Date: 02/28/1996
Regulation Medical Specialty: Cardiovascular
Device Name: ART-ASSIST MODEL AA-1000
Manufacturer: ACI MEDICAL, INC.
Device Classification Name: sleeve, limb, compressible
Regulation Number: 870.5800
Classification Product Code: JOW
Date Received: 05/27/1994
Decision Date: 02/28/1996
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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