Euro-American Marketing Group, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Euro-American Marketing Group, Inc. makes
Euro-American Marketing Group, Inc. manufactures the CardiPhone, a medical device designed for cardiac monitoring and telemetry, the Euramark 610 Photometer for clinical chemistry analysis, and the Murse Retractor, a surgical instrument used to hold back tissue during procedures.
The company’s products are regulated under FDA 510(k) clearance, with devices classified as Class I and Class II. The portfolio is listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Cardiophone Ref K894856
Regimes: 510(k) Registry: 510(k)Euramark 610 Photometer Ref K903164
Regimes: 510(k) Registry: 510(k)Murse Retractor Ref K882112
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Euro-American Marketing Group, Inc. have in the registry?
The registry currently lists 3 devices for Euro-American Marketing Group, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Euro-American Marketing Group, Inc.'s devices?
Among its 3 most recently registered devices, Euro-American Marketing Group, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Euro-American Marketing Group, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Euro-American Marketing Group, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Euro-American Marketing Group, Inc. in the registry?
The most recently registered devices listed for Euro-American Marketing Group, Inc. include CARDIOPHONE, EURAMARK 610 PHOTOMETER and MURSE RETRACTOR.