FDA 510(k), K940187, ENVOY GUIDING CATHETER
FDA 510(k), K940187, ENVOY GUIDING CATHETER
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510(K) Number: K940187
Device Name: ENVOY GUIDING CATHETER
Manufacturer:
Device Classification Name: Catheter, Percutaneous
Regulation Number: 870.1250
Classification Product Code: DQY
Date Received: 01/13/1994
Decision Date: 03/30/1994
Regulation Medical Specialty: Cardiovascular
Device Name: ENVOY GUIDING CATHETER
Manufacturer:
Device Classification Name: Catheter, Percutaneous
Regulation Number: 870.1250
Classification Product Code: DQY
Date Received: 01/13/1994
Decision Date: 03/30/1994
Regulation Medical Specialty: Cardiovascular