FDA 510(k), K133948, BARD(R) MONOPTY(R) DISPOSABLE CORE BIOPSY INSTRUMENT, BARD(R) MAX-CORE(R) DISPOSABLE CORE INSTRUMENT
FDA 510(k), K133948, BARD(R) MONOPTY(R) DISPOSABLE CORE BIOPSY INSTRUMENT, BARD(R) MAX-CORE(R) DISPOSABLE CORE INSTRUMENT
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510(K) Number: K133948
Device Name: BARD(R) MONOPTY(R) DISPOSABLE CORE BIOPSY INSTRUMENT, BARD(R) MAX-CORE(R) DISPOSABLE CORE INSTRUMENT
Manufacturer:
Device Classification Name: Instrument, Biopsy
Regulation Number: 876.1075
Classification Product Code: KNW
Date Received: 12/23/2013
Decision Date: 02/21/2014
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: BARD(R) MONOPTY(R) DISPOSABLE CORE BIOPSY INSTRUMENT, BARD(R) MAX-CORE(R) DISPOSABLE CORE INSTRUMENT
Manufacturer:
Device Classification Name: Instrument, Biopsy
Regulation Number: 876.1075
Classification Product Code: KNW
Date Received: 12/23/2013
Decision Date: 02/21/2014
Regulation Medical Specialty: Gastroenterology/Urology