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FDA 510(k), K042117, PROXIS SYSTEM, MODEL EPS 101
FDA 510(k), K042117, PROXIS SYSTEM, MODEL EPS 101
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510(K) Number: K042117
Device Name: PROXIS SYSTEM, MODEL EPS 101
Manufacturer: VELOCIMED INC.
Device Classification Name: catheter, percutaneous
Regulation Number: 870.1250
Classification Product Code: DQY
Date Received: 08/05/2004
Decision Date: 01/07/2005
Regulation Medical Specialty: Cardiovascular
Device Name: PROXIS SYSTEM, MODEL EPS 101
Manufacturer: VELOCIMED INC.
Device Classification Name: catheter, percutaneous
Regulation Number: 870.1250
Classification Product Code: DQY
Date Received: 08/05/2004
Decision Date: 01/07/2005
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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