The following data is part of a premarket notification filed by Conmed Corporation with the FDA for Cable, Transducer, Model 2400gn.
| Device ID | K083448 |
| 510k Number | K083448 |
| Device Name: | CABLE, TRANSDUCER, MODEL 2400GN |
| Classification | Oximeter |
| Applicant | CONMED CORPORATION 525 FRENCH RD. Utica, NY 13502 |
| Contact | Sarah Rizk |
| Correspondent | Sarah Rizk CONMED CORPORATION 525 FRENCH RD. Utica, NY 13502 |
| Product Code | DQA |
| CFR Regulation Number | 870.2700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-11-21 |
| Decision Date | 2009-08-20 |
| Summary: | summary |