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 |