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FDA 510(k), K131272, SIREN EPCR SUITE
FDA 510(k), K131272, SIREN EPCR SUITE
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510(K) Number: K131272
Device Name: SIREN EPCR SUITE
Manufacturer: MEDUSA MEDICAL TECHNOLOGIES INC.
Device Classification Name: display, cathode-ray tube, medical
Regulation Number: 870.2450
Classification Product Code: DXJ
Date Received: 05/03/2013
Decision Date: 01/03/2014
Regulation Medical Specialty: Cardiovascular
Device Name: SIREN EPCR SUITE
Manufacturer: MEDUSA MEDICAL TECHNOLOGIES INC.
Device Classification Name: display, cathode-ray tube, medical
Regulation Number: 870.2450
Classification Product Code: DXJ
Date Received: 05/03/2013
Decision Date: 01/03/2014
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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