FDA 510(k), K133849, VANTERA CLINICAL ANALYZER
FDA 510(k), K133849, VANTERA CLINICAL ANALYZER
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510(K) Number: K133849
Device Name: VANTERA CLINICAL ANALYZER
Manufacturer: LIPOSCIENCE
Device Classification Name: instrumentation for clinical multiplex test systems
Regulation Number: 862.2570
Classification Product Code: NSU
Date Received: 12/19/2013
Decision Date: 10/22/2014
Regulation Medical Specialty: Clinical Chemistry
Device Name: VANTERA CLINICAL ANALYZER
Manufacturer: LIPOSCIENCE
Device Classification Name: instrumentation for clinical multiplex test systems
Regulation Number: 862.2570
Classification Product Code: NSU
Date Received: 12/19/2013
Decision Date: 10/22/2014
Regulation Medical Specialty: Clinical Chemistry