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FDA 510(k), K071234, ACUNAV DIAGNOSTIC ULTRASOUND CATHETER 8F AND 10F
FDA 510(k), K071234, ACUNAV DIAGNOSTIC ULTRASOUND CATHETER 8F AND 10F
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510(K) Number: K071234
Device Name: ACUNAV DIAGNOSTIC ULTRASOUND CATHETER 8F AND 10F
Manufacturer: SIEMENS MEDICAL SOLUTIONS USA, INC.
Device Classification Name: catheter, ultrasound, intravascular
Regulation Number: 870.1200
Classification Product Code: OBJ
Date Received: 05/03/2007
Decision Date: 06/29/2007
Regulation Medical Specialty: Cardiovascular
Device Name: ACUNAV DIAGNOSTIC ULTRASOUND CATHETER 8F AND 10F
Manufacturer: SIEMENS MEDICAL SOLUTIONS USA, INC.
Device Classification Name: catheter, ultrasound, intravascular
Regulation Number: 870.1200
Classification Product Code: OBJ
Date Received: 05/03/2007
Decision Date: 06/29/2007
Regulation Medical Specialty: Cardiovascular
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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