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 |