The following data is part of a premarket notification filed by Biolase Technology, Inc. with the FDA for Diolase 10s.
| Device ID | K121327 |
| 510k Number | K121327 |
| Device Name: | DIOLASE 10S |
| Classification | Powered Laser Surgical Instrument |
| Applicant | BIOLASE TECHNOLOGY, INC. 4 CROMWELL Irvine, CA 92618 -1816 |
| Contact | Robert Yang |
| Correspondent | Robert Yang BIOLASE TECHNOLOGY, INC. 4 CROMWELL Irvine, CA 92618 -1816 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-05-02 |
| Decision Date | 2013-02-01 |
| Summary: | summary |