Ametek, Inc.
Also registered as Ametek
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Dynamometer - Model Fce And Model Msc Ref K042889
Regimes: 510(k) Registry: 510(k)Carbon Dioxide Analyzer (Model Cd-3A) Ref K942113
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ametek, Inc. have in the registry?
The registry currently lists 3 devices for Ametek, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ametek, Inc.'s devices?
Among its 3 most recently registered devices, Ametek, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Ametek, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Ametek, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ametek, Inc. in the registry?
The most recently registered devices listed for Ametek, Inc. include DYNAMOMETER - MODEL FCE AND MODEL MSC, CARBON DIOXIDE ANALYZER (MODEL CD-3A) and GASEOUS OXYGEN ANALYZER (MODEL S-3A) MODIFICATION.