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FDA 510(k), K833112, TUBING FOR CARDIOPULMONARY BYPASS
FDA 510(k), K833112, TUBING FOR CARDIOPULMONARY BYPASS
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510(K) Number: K833112
Device Name: TUBING FOR CARDIOPULMONARY BYPASS
Manufacturer: CARDIO MED SUPPLIES, INC.
Device Classification Name: catheter, cannula and tubing, vascular, cardiopulmonary bypass
Regulation Number: 870.4210
Classification Product Code: DWF
Date Received: 08/16/1983
Decision Date: 11/28/1983
Regulation Medical Specialty: Cardiovascular
Device Name: TUBING FOR CARDIOPULMONARY BYPASS
Manufacturer: CARDIO MED SUPPLIES, INC.
Device Classification Name: catheter, cannula and tubing, vascular, cardiopulmonary bypass
Regulation Number: 870.4210
Classification Product Code: DWF
Date Received: 08/16/1983
Decision Date: 11/28/1983
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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