FDA 510(k), K091703, HD GUIDE CATHETER, MODEL 90019, 90022, 90023, 90120, 90121, 90130, 90131
FDA 510(k), K091703, HD GUIDE CATHETER, MODEL 90019, 90022, 90023, 90120, 90121, 90130, 90131
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$149.00 USD
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$149.00 USD
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510(K) Number: K091703
Device Name: HD GUIDE CATHETER, MODEL 90019, 90022, 90023, 90120, 90121, 90130, 90131
Manufacturer: CONCENTRIC MEDICAL, INC.
Device Classification Name: aspiration thrombectomy catheter
Regulation Number: 870.5150
Classification Product Code: QEZ
Date Received: 06/10/2009
Decision Date: 10/14/2009
Regulation Medical Specialty: Cardiovascular
Device Name: HD GUIDE CATHETER, MODEL 90019, 90022, 90023, 90120, 90121, 90130, 90131
Manufacturer: CONCENTRIC MEDICAL, INC.
Device Classification Name: aspiration thrombectomy catheter
Regulation Number: 870.5150
Classification Product Code: QEZ
Date Received: 06/10/2009
Decision Date: 10/14/2009
Regulation Medical Specialty: Cardiovascular