The following data is part of a premarket notification filed by Medax Srl Unipersonale with the FDA for New Medax Biopsy Systems.
Device ID | K142125 |
510k Number | K142125 |
Device Name: | New Medax Biopsy Systems |
Classification | Instrument, Biopsy |
Applicant | MEDAX SRL UNIPERSONALE VIA R. Piva 1/A Poggio Rusco, IT 46025 |
Contact | Stefano Cavalieri |
Correspondent | Serena Coronati Coronati Consutling Sas VIA LUIGI GAVIOLI, 3 Mirandola, IT 41307 |
Product Code | KNW |
CFR Regulation Number | 876.1075 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-08-04 |
Decision Date | 2015-12-22 |