FDA 510(k), K052989, DP240 240 HOUR DOPPLER PROBE
FDA 510(k), K052989, DP240 240 HOUR DOPPLER PROBE
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510(K) Number: K052989
Device Name: DP240 240 HOUR DOPPLER PROBE
Manufacturer: DELTEX MEDICAL
Device Classification Name: probe, blood-flow, extravascular
Regulation Number: 870.2120
Classification Product Code: DPT
Date Received: 10/24/2005
Decision Date: 03/08/2006
Regulation Medical Specialty: Cardiovascular
Device Name: DP240 240 HOUR DOPPLER PROBE
Manufacturer: DELTEX MEDICAL
Device Classification Name: probe, blood-flow, extravascular
Regulation Number: 870.2120
Classification Product Code: DPT
Date Received: 10/24/2005
Decision Date: 03/08/2006
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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