The following data is part of a premarket notification filed by Premier Laser Systems, Inc. with the FDA for Aurora Hl.
| Device ID | K992374 |
| 510k Number | K992374 |
| Device Name: | AURORA HL |
| Classification | Powered Laser Surgical Instrument |
| Applicant | PREMIER LASER SYSTEMS, INC. #3 MORGAN Irvine, CA 92618 |
| Contact | Beth A Roberts |
| Correspondent | Beth A Roberts PREMIER LASER SYSTEMS, INC. #3 MORGAN Irvine, CA 92618 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-07-15 |
| Decision Date | 1999-09-22 |