The following data is part of a premarket notification filed by Kerr Corporation (danbury) with the FDA for Handpiece, Lift, Endo.
| Device ID | K780213 |
| 510k Number | K780213 |
| Device Name: | HANDPIECE, LIFT, ENDO |
| Classification | Handpiece, Contra- And Right-angle Attachment, Dental |
| Applicant | KERR CORPORATION (DANBURY) 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EGS |
| CFR Regulation Number | 872.4200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-02-08 |
| Decision Date | 1978-02-17 |