The following data is part of a premarket notification filed by Trimedyne, Inc. with the FDA for Trimedyne Model 1210 Omnipulse Holmium Lase Syst.
| Device ID | K925124 |
| 510k Number | K925124 |
| Device Name: | TRIMEDYNE MODEL 1210 OMNIPULSE HOLMIUM LASE SYST |
| Classification | Powered Laser Surgical Instrument |
| Applicant | TRIMEDYNE, INC. 47201 LAKEVIEW BLVD. P.O. BOX 5120 Fremont, CA 94537 |
| Contact | Paul S Kramsky |
| Correspondent | Paul S Kramsky TRIMEDYNE, INC. 47201 LAKEVIEW BLVD. P.O. BOX 5120 Fremont, CA 94537 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-10-13 |
| Decision Date | 1994-03-01 |