FDA 510(k), K063204, SPIDERFX EMBOLIC PROTECTION DEVICE
FDA 510(k), K063204, SPIDERFX EMBOLIC PROTECTION DEVICE
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$149.00 USD
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510(K) Number: K063204
Device Name: SPIDERFX EMBOLIC PROTECTION DEVICE
Manufacturer:
Device Classification Name: Temporary Carotid Catheter For Embolic Capture
Regulation Number: 870.1250
Classification Product Code: NTE
Date Received: 10/23/2006
Decision Date: 11/14/2006
Regulation Medical Specialty: Cardiovascular
Device Name: SPIDERFX EMBOLIC PROTECTION DEVICE
Manufacturer:
Device Classification Name: Temporary Carotid Catheter For Embolic Capture
Regulation Number: 870.1250
Classification Product Code: NTE
Date Received: 10/23/2006
Decision Date: 11/14/2006
Regulation Medical Specialty: Cardiovascular