The following data is part of a premarket notification filed by Hamilton Medical Ag with the FDA for Hamilton-t1,hamilton-c1.
| Device ID | K140939 |
| 510k Number | K140939 |
| Device Name: | HAMILTON-T1,HAMILTON-C1 |
| Classification | Ventilator, Continuous, Facility Use |
| Applicant | HAMILTON MEDICAL AG VIA CRUSCH 8 Bonaduz, Grisons, CH 7402 |
| Contact | Frederike Bruehschwein |
| Correspondent | Frederike Bruehschwein HAMILTON MEDICAL AG VIA CRUSCH 8 Bonaduz, Grisons, CH 7402 |
| Product Code | CBK |
| CFR Regulation Number | 868.5895 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-04-11 |
| Decision Date | 2015-09-02 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 07630002806091 | K140939 | 000 |
| 07630002801850 | K140939 | 000 |
| 07630002800747 | K140939 | 000 |