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FDA 510(k), K133539, TOTAL ACROSS
FDA 510(k), K133539, TOTAL ACROSS
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510(K) Number: K133539
Device Name: TOTAL ACROSS
Manufacturer: MEDTRONIC VASCULAR
Device Classification Name: catheter, percutaneous
Regulation Number: 870.1250
Classification Product Code: DQY
Date Received: 11/18/2013
Decision Date: 03/26/2014
Regulation Medical Specialty: Cardiovascular
Device Name: TOTAL ACROSS
Manufacturer: MEDTRONIC VASCULAR
Device Classification Name: catheter, percutaneous
Regulation Number: 870.1250
Classification Product Code: DQY
Date Received: 11/18/2013
Decision Date: 03/26/2014
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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