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FDA 510(k), K072776, THE CROSSER SYSTEM
FDA 510(k), K072776, THE CROSSER SYSTEM
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$149.00 USD
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$149.00 USD
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510(K) Number: K072776
Device Name: THE CROSSER SYSTEM
Manufacturer:
Device Classification Name: Catheter For Crossing Total Occlusions
Regulation Number: 870.1250
Classification Product Code: PDU
Date Received: 09/28/2007
Decision Date: 12/07/2007
Regulation Medical Specialty: Cardiovascular
Device Name: THE CROSSER SYSTEM
Manufacturer:
Device Classification Name: Catheter For Crossing Total Occlusions
Regulation Number: 870.1250
Classification Product Code: PDU
Date Received: 09/28/2007
Decision Date: 12/07/2007
Regulation Medical Specialty: Cardiovascular
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