The following data is part of a premarket notification filed by Biolase Technology, Inc. with the FDA for Oculase Md.
| Device ID | K052354 |
| 510k Number | K052354 |
| Device Name: | OCULASE MD |
| Classification | Powered Laser Surgical Instrument |
| Applicant | BIOLASE TECHNOLOGY, INC. 981 CALLE AMANECER San Clemente, CA 92673 |
| Contact | Jeffrey W Jones |
| Correspondent | Jeffrey W Jones BIOLASE TECHNOLOGY, INC. 981 CALLE AMANECER San Clemente, CA 92673 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-08-29 |
| Decision Date | 2006-07-05 |
| Summary: | summary |