WATERLASE MD

Powered Laser Surgical Instrument

BIOLASE TECHNOLOGY, INC.

The following data is part of a premarket notification filed by Biolase Technology, Inc. with the FDA for Waterlase Md.

Pre-market Notification Details

Device IDK090181
510k NumberK090181
Device Name:WATERLASE MD
ClassificationPowered Laser Surgical Instrument
Applicant BIOLASE TECHNOLOGY, INC. 4 CROMWELL Irvine,  CA  92618 -1816
ContactIoana Rizoiu
CorrespondentIoana Rizoiu
BIOLASE TECHNOLOGY, INC. 4 CROMWELL Irvine,  CA  92618 -1816
Product CodeGEX  
CFR Regulation Number878.4810 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2009-01-26
Decision Date2009-02-11
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
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

Trademark Results [WATERLASE MD]

Mark Image

Registration | Serial
Company
Trademark
Application Date
WATERLASE MD
WATERLASE MD
77185280 3587923 Live/Registered
BIOLASE, INC.
2007-05-18

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