The following data is part of a premarket notification filed by Conmed Corporation with the FDA for Vcare Retractor/elevator.
| Device ID | K071907 |
| 510k Number | K071907 |
| Device Name: | VCARE RETRACTOR/ELEVATOR |
| Classification | Cannula, Manipulator/injector, Uterine |
| Applicant | CONMED CORPORATION 525 FRENCH RD. Utica, NY 13502 |
| Contact | Brian Killoran |
| Correspondent | Brian Killoran CONMED CORPORATION 525 FRENCH RD. Utica, NY 13502 |
| Product Code | LKF |
| CFR Regulation Number | 884.4530 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-07-10 |
| Decision Date | 2007-10-05 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20653405061820 | K071907 | 000 |
| 20653405061813 | K071907 | 000 |
| 20653405061806 | K071907 | 000 |
| 20653405061790 | K071907 | 000 |