FDA 510(k), K040067, CLIRPATH EXCIMER LASER CATHETER
FDA 510(k), K040067, CLIRPATH EXCIMER LASER CATHETER
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$149.00 USD
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510(K) Number: K040067
Device Name: CLIRPATH EXCIMER LASER CATHETER
Manufacturer:
Device Classification Name: Catheter For Crossing Total Occlusions
Regulation Number: 870.1250
Classification Product Code: PDU
Date Received: 01/14/2004
Decision Date: 04/27/2004
Regulation Medical Specialty: Cardiovascular
Device Name: CLIRPATH EXCIMER LASER CATHETER
Manufacturer:
Device Classification Name: Catheter For Crossing Total Occlusions
Regulation Number: 870.1250
Classification Product Code: PDU
Date Received: 01/14/2004
Decision Date: 04/27/2004
Regulation Medical Specialty: Cardiovascular