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FDA 510(k), K874706, MODIFIED SIMPSON PERIPHERAL ATHEROCATH
FDA 510(k), K874706, MODIFIED SIMPSON PERIPHERAL ATHEROCATH
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510(K) Number: K874706
Device Name: MODIFIED SIMPSON PERIPHERAL ATHEROCATH
Manufacturer: JAMES F PFEIFFER
Device Classification Name: Catheter, Angioplasty, Peripheral, Transluminal
Regulation Number: LIT
Classification Product Code: 11/04/1987
Date Received: 01/04/1988
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: MODIFIED SIMPSON PERIPHERAL ATHEROCATH
Manufacturer: JAMES F PFEIFFER
Device Classification Name: Catheter, Angioplasty, Peripheral, Transluminal
Regulation Number: LIT
Classification Product Code: 11/04/1987
Date Received: 01/04/1988
Decision Date: Substantially Equivalent (SESE)
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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