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FDA 510(k), K864567, 40CC PERCUTANEOUS FURL DOU. LUMEN BALLOON CATHETER
FDA 510(k), K864567, 40CC PERCUTANEOUS FURL DOU. LUMEN BALLOON CATHETER
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510(K) Number: K864567
Device Name: 40CC PERCUTANEOUS FURL DOU. LUMEN BALLOON CATHETER
Manufacturer: ARIES MEDICAL, INC.
Device Classification Name: system, balloon, intra-aortic and control
Regulation Number: 870.3535
Classification Product Code: DSP
Date Received: 11/19/1986
Decision Date: 05/12/1987
Regulation Medical Specialty: Cardiovascular
Device Name: 40CC PERCUTANEOUS FURL DOU. LUMEN BALLOON CATHETER
Manufacturer: ARIES MEDICAL, INC.
Device Classification Name: system, balloon, intra-aortic and control
Regulation Number: 870.3535
Classification Product Code: DSP
Date Received: 11/19/1986
Decision Date: 05/12/1987
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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