Dms Products, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 6
What Dms Products, Inc. makes
Dms Products, Inc. manufactures microbiological diagnostic reagents and identification kits, including rapid test systems for detecting bacterial pathogens such as *E. coli*, *Staphylococcus*, and urinary tract infections, as well as culture media and biochemical reagents for bacterial identification.
The company’s products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. These devices are intended for in vitro diagnostic use and are registered in the U.S. market.
Catalogue
Rapidec Coli Ref K890626
510(k) 510(k)Api 50 Chb (Culture Media) Ref K854732
510(k) 510(k)Rapidec Ur Ref K894805
510(k) 510(k)James Reagent Ref K890625
510(k) 510(k)Rapidec Staph Ref K891004
510(k) 510(k)- 510(k) 510(k)
Frequently asked questions
How many devices does Dms Products, Inc. have in the registry?
The registry currently lists 6 devices for Dms Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dms Products, Inc.'s devices?
Among its 6 most recently registered devices, Dms Products, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Dms Products, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Dms Products, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dms Products, Inc. in the registry?
The most recently registered devices listed for Dms Products, Inc. include RAPIDEC COLI, API 50 CHB (CULTURE MEDIA), RAPIDEC UR and JAMES REAGENT.