The following data is part of a premarket notification filed by Thornhill Research Inc. with the FDA for Madm.
Device ID | K140264 |
510k Number | K140264 |
Device Name: | MADM |
Classification | Gas-machine, Anesthesia |
Applicant | THORNHILL RESEARCH INC. 210 Dundas St. West Suite 200 Toronto, Ontario, CA M5g 2e8 |
Contact | Cliff Ansel |
Correspondent | Cliff Ansel THORNHILL RESEARCH INC. 210 Dundas St. West Suite 200 Toronto, Ontario, CA M5g 2e8 |
Product Code | BSZ |
CFR Regulation Number | 868.5160 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-02-03 |
Decision Date | 2015-01-05 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
18071411246416 | K140264 | 000 |
10807141000091 | K140264 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MADM 86589553 5350960 Live/Registered |
Thornhill Research Inc. 2015-04-07 |