New Medax Biopsy Systems

Instrument, Biopsy

MEDAX SRL UNIPERSONALE

The following data is part of a premarket notification filed by Medax Srl Unipersonale with the FDA for New Medax Biopsy Systems.

Pre-market Notification Details

Device IDK142125
510k NumberK142125
Device Name:New Medax Biopsy Systems
ClassificationInstrument, Biopsy
Applicant MEDAX SRL UNIPERSONALE VIA R. Piva 1/A Poggio Rusco,  IT 46025
ContactStefano Cavalieri
CorrespondentSerena Coronati
Coronati Consutling Sas VIA LUIGI GAVIOLI, 3 Mirandola,  IT 41307
Product CodeKNW  
CFR Regulation Number876.1075 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2014-08-04
Decision Date2015-12-22

NIH GUDID Devices

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