MADM

Gas-machine, Anesthesia

THORNHILL RESEARCH INC.

The following data is part of a premarket notification filed by Thornhill Research Inc. with the FDA for Madm.

Pre-market Notification Details

Device IDK140264
510k NumberK140264
Device Name:MADM
ClassificationGas-machine, Anesthesia
Applicant THORNHILL RESEARCH INC. 210 Dundas St. West Suite 200 Toronto, Ontario,  CA M5g 2e8
ContactCliff Ansel
CorrespondentCliff Ansel
THORNHILL RESEARCH INC. 210 Dundas St. West Suite 200 Toronto, Ontario,  CA M5g 2e8
Product CodeBSZ  
CFR Regulation Number868.5160 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2014-02-03
Decision Date2015-01-05
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
18071411246416 K140264 000
10807141000091 K140264 000

Trademark Results [MADM]

Mark Image

Registration | Serial
Company
Trademark
Application Date
MADM
MADM
86589553 5350960 Live/Registered
Thornhill Research Inc.
2015-04-07

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.