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FDA 510(k), K922368, PERIFLUX PF4001 LASER DOPPLER FLOWMETER
FDA 510(k), K922368, PERIFLUX PF4001 LASER DOPPLER FLOWMETER
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510(K) Number: K922368
Device Name: PERIFLUX PF4001 LASER DOPPLER FLOWMETER
Manufacturer: OYSTEIN LIND
Device Classification Name: Flowmeter, Blood, Cardiovascular
Regulation Number: DPW
Classification Product Code: 05/20/1992
Date Received: 02/03/1993
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: PERIFLUX PF4001 LASER DOPPLER FLOWMETER
Manufacturer: OYSTEIN LIND
Device Classification Name: Flowmeter, Blood, Cardiovascular
Regulation Number: DPW
Classification Product Code: 05/20/1992
Date Received: 02/03/1993
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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