The following data is part of a premarket notification filed by Trimedyne, Inc. with the FDA for Lateralase.
| Device ID | K920625 |
| 510k Number | K920625 |
| Device Name: | LATERALASE |
| Classification | Powered Laser Surgical Instrument |
| Applicant | TRIMEDYNE, INC. 2801 BARRANCA RD. Irvine, CA 92714 -5114 |
| Contact | Paul S Kramsky |
| Correspondent | Paul S Kramsky TRIMEDYNE, INC. 2801 BARRANCA RD. Irvine, CA 92714 -5114 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-02-12 |
| Decision Date | 1992-04-02 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() LATERALASE 74159126 2557504 Dead/Cancelled |
Trimedyne Inc. 1991-04-15 |
![]() LATERALASE 74105660 not registered Dead/Abandoned |
Everett, Royice B. 1990-10-15 |