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FDA 510(k), K920844, PIM 1.0 LASER DOPPLER PERFUSION IMAGER
FDA 510(k), K920844, PIM 1.0 LASER DOPPLER PERFUSION IMAGER
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510(K) Number: K920844
Device Name: PIM 1.0 LASER DOPPLER PERFUSION IMAGER
Manufacturer: GERT NILSSON
Device Classification Name: Flowmeter, Blood, Cardiovascular
Regulation Number: DPW
Classification Product Code: 02/24/1992
Date Received: 07/21/1992
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: PIM 1.0 LASER DOPPLER PERFUSION IMAGER
Manufacturer: GERT NILSSON
Device Classification Name: Flowmeter, Blood, Cardiovascular
Regulation Number: DPW
Classification Product Code: 02/24/1992
Date Received: 07/21/1992
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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