The following data is part of a premarket notification filed by Biolase Technology, Inc. with the FDA for Waterlase Md.
| Device ID | K090181 |
| 510k Number | K090181 |
| Device Name: | WATERLASE MD |
| Classification | Powered Laser Surgical Instrument |
| Applicant | BIOLASE TECHNOLOGY, INC. 4 CROMWELL Irvine, CA 92618 -1816 |
| Contact | Ioana Rizoiu |
| Correspondent | Ioana Rizoiu BIOLASE TECHNOLOGY, INC. 4 CROMWELL Irvine, CA 92618 -1816 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-01-26 |
| Decision Date | 2009-02-11 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00647529002490 | K090181 | 000 |
| 00647529000526 | K090181 | 000 |
| 00647529000540 | K090181 | 000 |
| 00647529000571 | K090181 | 000 |
| 00647529000588 | K090181 | 000 |
| 00647529001554 | K090181 | 000 |
| 00647529001615 | K090181 | 000 |
| 00647529001622 | K090181 | 000 |
| 00647529002285 | K090181 | 000 |
| 00647529002469 | K090181 | 000 |
| 00647529002674 | K090181 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() WATERLASE MD 77185280 3587923 Live/Registered |
BIOLASE, INC. 2007-05-18 |