Dresser Argus, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Dresser Argus, Inc. makes
Dresser Argus, Inc. manufactures investigation kits for sexual assault determination, including the DRESSER ARGUS P/N 1818.
The company's devices are listed in the FDA 510(k) registry and include Class II and Class U devices. Dresser Argus, Inc. is based in the US.
Catalogue
Investigation Kit, Sexual Assault Determination Ref K880208
510(k) 510(k)Dresser Argus P/N 1818 Ref K905304
510(k) 510(k)
Frequently asked questions
How many devices does Dresser Argus, Inc. have in the registry?
The registry currently lists 2 devices for Dresser Argus, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dresser Argus, Inc.'s devices?
Among its 2 most recently registered devices, Dresser Argus, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Dresser Argus, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Dresser Argus, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dresser Argus, Inc. in the registry?
The most recently registered devices listed for Dresser Argus, Inc. include INVESTIGATION KIT, SEXUAL ASSAULT DETERMINATION and DRESSER ARGUS P/N 1818.