The following data is part of a premarket notification filed by Hamilton Medical Ag with the FDA for Hamilton-c1.
Device ID | K120574 |
510k Number | K120574 |
Device Name: | HAMILTON-C1 |
Classification | Ventilator, Continuous, Facility Use |
Applicant | HAMILTON MEDICAL AG VIA CRUSCH 8 Bonaduz, CH Ch-7402 |
Contact | Ralph Aguila |
Correspondent | Ralph Aguila HAMILTON MEDICAL AG VIA CRUSCH 8 Bonaduz, CH Ch-7402 |
Product Code | CBK |
CFR Regulation Number | 868.5895 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-02-27 |
Decision Date | 2012-05-30 |
Summary: | summary |