FDA 510(k), K932725, B-D ULTRA FINE(R) LANCET
FDA 510(k), K932725, B-D ULTRA FINE(R) LANCET
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$149.00 USD
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$149.00 USD
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510(K) Number: K932725
Device Name: B-D ULTRA FINE(R) LANCET
Manufacturer: RUSSELL ARNSBERGER
Device Classification Name: Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
Regulation Number: FMK
Classification Product Code: 06/07/1993
Date Received: 07/23/1993
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: B-D ULTRA FINE(R) LANCET
Manufacturer: RUSSELL ARNSBERGER
Device Classification Name: Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
Regulation Number: FMK
Classification Product Code: 06/07/1993
Date Received: 07/23/1993
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery