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FDA 510(k), K895753, BREVET DISPOSABLE CONNECTORS
FDA 510(k), K895753, BREVET DISPOSABLE CONNECTORS
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510(K) Number: K895753
Device Name: BREVET DISPOSABLE CONNECTORS
Manufacturer: TIMOTHY DIAMOND
Device Classification Name: Catheter, Percutaneous
Regulation Number: DQY
Classification Product Code: KXA
Date Received: 09/26/1989
Decision Date: 11/14/1989
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: BREVET DISPOSABLE CONNECTORS
Manufacturer: TIMOTHY DIAMOND
Device Classification Name: Catheter, Percutaneous
Regulation Number: DQY
Classification Product Code: KXA
Date Received: 09/26/1989
Decision Date: 11/14/1989
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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