The following data is part of a premarket notification filed by Conmed Corporation with the FDA for Detachatip Iii.
| Device ID | K123260 |
| 510k Number | K123260 |
| Device Name: | DETACHATIP III |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | CONMED CORPORATION 525 FRENCH RD. Utica, NY 13502 |
| Contact | Lisa Anderson |
| Correspondent | Lisa Anderson CONMED CORPORATION 525 FRENCH RD. Utica, NY 13502 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-10-18 |
| Decision Date | 2012-12-21 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 40653405061787 | K123260 | 000 |
| 40653405061626 | K123260 | 000 |
| 40653405061619 | K123260 | 000 |
| 40653405061602 | K123260 | 000 |
| 40653405061596 | K123260 | 000 |
| 40653405061589 | K123260 | 000 |
| 40653405061572 | K123260 | 000 |
| 40653405061565 | K123260 | 000 |
| 40653405061558 | K123260 | 000 |
| 40653405061541 | K123260 | 000 |
| 40653405061534 | K123260 | 000 |
| 30653405063814 | K123260 | 000 |
| 30653405063807 | K123260 | 000 |
| 40653405061640 | K123260 | 000 |
| 40653405061657 | K123260 | 000 |
| 40653405061770 | K123260 | 000 |
| 40653405061763 | K123260 | 000 |
| 40653405061756 | K123260 | 000 |
| 40653405061749 | K123260 | 000 |
| 40653405061732 | K123260 | 000 |
| 40653405061725 | K123260 | 000 |
| 40653405061718 | K123260 | 000 |
| 40653405061701 | K123260 | 000 |
| 40653405061695 | K123260 | 000 |
| 30653405061681 | K123260 | 000 |
| 40653405061671 | K123260 | 000 |
| 40653405061664 | K123260 | 000 |
| 20653405061684 | K123260 | 000 |