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FDA 510(k), K103110, MINI TREK(TM) RX AND TREK(TM) RX CORONARY DILATATION CATHETER MINI TREK(TM) OTW AND TREK(TM) OTW DILATATION CATHETER
FDA 510(k), K103110, MINI TREK(TM) RX AND TREK(TM) RX CORONARY DILATATION CATHETER MINI TREK(TM) OTW AND TREK(TM) OTW DILATATION CATHETER
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$149.00 USD
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$149.00 USD
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510(K) Number: K103110
Device Name: MINI TREK(TM) RX AND TREK(TM) RX CORONARY DILATATION CATHETER MINI TREK(TM) OTW AND TREK(TM) OTW DILATATION CATHETER
Manufacturer: ABBOTT VASCULAR-CARDIAC THERAPIES
Device Classification Name: catheters, transluminal coronary angioplasty, percutaneous
Regulation Number: 870.5100
Classification Product Code: LOX
Date Received: 10/08/2010
Decision Date: 01/10/2011
Regulation Medical Specialty: Cardiovascular
Device Name: MINI TREK(TM) RX AND TREK(TM) RX CORONARY DILATATION CATHETER MINI TREK(TM) OTW AND TREK(TM) OTW DILATATION CATHETER
Manufacturer: ABBOTT VASCULAR-CARDIAC THERAPIES
Device Classification Name: catheters, transluminal coronary angioplasty, percutaneous
Regulation Number: 870.5100
Classification Product Code: LOX
Date Received: 10/08/2010
Decision Date: 01/10/2011
Regulation Medical Specialty: Cardiovascular
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