FDA 510(k), K872048, TRANSONIC FLOWMETER
FDA 510(k), K872048, TRANSONIC FLOWMETER
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510(K) Number: K872048
Device Name: TRANSONIC FLOWMETER
Manufacturer: SHAWN P CREIGHTON
Device Classification Name: Flowmeter, Blood, Cardiovascular
Regulation Number: DPW
Classification Product Code: 05/28/1987
Date Received: 06/21/1988
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: TRANSONIC FLOWMETER
Manufacturer: SHAWN P CREIGHTON
Device Classification Name: Flowmeter, Blood, Cardiovascular
Regulation Number: DPW
Classification Product Code: 05/28/1987
Date Received: 06/21/1988
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
- 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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