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FDA 510(k), K905232, MOOR LASER BLOOD FLOW MONITOR MBF3
FDA 510(k), K905232, MOOR LASER BLOOD FLOW MONITOR MBF3
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$89.00 USD
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510(K) Number: K905232
Device Name: MOOR LASER BLOOD FLOW MONITOR MBF3
Manufacturer: N. J BARNETT
Device Classification Name: Powered Laser Surgical Instrument
Regulation Number: GEX
Classification Product Code: KXA
Date Received: 11/20/1990
Decision Date: 01/11/1991
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: MOOR LASER BLOOD FLOW MONITOR MBF3
Manufacturer: N. J BARNETT
Device Classification Name: Powered Laser Surgical Instrument
Regulation Number: GEX
Classification Product Code: KXA
Date Received: 11/20/1990
Decision Date: 01/11/1991
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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