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FDA 510(k), K871011, SIMPSON PERIPHERAL ATHEROCATH(TM)
FDA 510(k), K871011, SIMPSON PERIPHERAL ATHEROCATH(TM)
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510(K) Number: K871011
Device Name: SIMPSON PERIPHERAL ATHEROCATH(TM)
Manufacturer: JAMES F PFEIFFER
Device Classification Name: Catheter, Angioplasty, Peripheral, Transluminal
Regulation Number: LIT
Classification Product Code: KXA
Date Received: 03/13/1987
Decision Date: 05/14/1987
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: SIMPSON PERIPHERAL ATHEROCATH(TM)
Manufacturer: JAMES F PFEIFFER
Device Classification Name: Catheter, Angioplasty, Peripheral, Transluminal
Regulation Number: LIT
Classification Product Code: KXA
Date Received: 03/13/1987
Decision Date: 05/14/1987
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
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