The following data is part of a premarket notification filed by Sharplan Lasers, Inc. with the FDA for Sharplan Series 2900 Synthetic Contact Tips.
| Device ID | K894210 |
| 510k Number | K894210 |
| Device Name: | SHARPLAN SERIES 2900 SYNTHETIC CONTACT TIPS |
| Classification | Powered Laser Surgical Instrument |
| Applicant | SHARPLAN LASERS, INC. COLUMBIA SQUARE 555 THIRTEENTH STREET NW Washington, DC 20004 |
| Contact | Jonathan Kahan |
| Correspondent | Jonathan Kahan SHARPLAN LASERS, INC. COLUMBIA SQUARE 555 THIRTEENTH STREET NW Washington, DC 20004 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-06-19 |
| Decision Date | 1989-08-10 |