The following data is part of a premarket notification filed by Biolase Technology, Inc. with the FDA for Waterlase Md Turbo Plus Model 7200xxx.
Device ID | K101658 |
510k Number | K101658 |
Device Name: | WATERLASE MD TURBO PLUS MODEL 7200XXX |
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 | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-06-11 |
Decision Date | 2010-08-11 |
Summary: | summary |