The following data is part of a premarket notification filed by Sharplan Lasers, Inc. with the FDA for Sharplan Models 719/719sr/719sl Colposlad Cos Su.
| Device ID | K881953 |
| 510k Number | K881953 |
| Device Name: | SHARPLAN MODELS 719/719SR/719SL COLPOSLAD COS SU |
| Classification | Powered Laser Surgical Instrument |
| Applicant | SHARPLAN LASERS, INC. 1 PEARL COURT Allendale, NJ 07401 |
| Contact | Dalton |
| Correspondent | Dalton SHARPLAN LASERS, INC. 1 PEARL COURT Allendale, NJ 07401 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-05-10 |
| Decision Date | 1988-06-03 |