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FDA 510(k), K760894, VACUUM RELIEF VALVE
FDA 510(k), K760894, VACUUM RELIEF VALVE
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510(K) Number: K760894
Device Name: VACUUM RELIEF VALVE
Manufacturer: DELTA MEDICAL INDUSTRIES
Device Classification Name: suction control, intracardiac, cardiopulmonary bypass
Regulation Number: 870.4430
Classification Product Code: DWD
Date Received: 10/26/1976
Decision Date: 12/09/1976
Regulation Medical Specialty: Cardiovascular
Device Name: VACUUM RELIEF VALVE
Manufacturer: DELTA MEDICAL INDUSTRIES
Device Classification Name: suction control, intracardiac, cardiopulmonary bypass
Regulation Number: 870.4430
Classification Product Code: DWD
Date Received: 10/26/1976
Decision Date: 12/09/1976
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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