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 |