Health Care Products, Inc.
United Statesfrom the FDA registration address FDA FEI 3006073016
- Devices
- 5
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Optivent Ref K963793
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3006073016
- DUNS number
- 613031009
- Address
- 410 NISCO ST., COLDWATER, OH, 45828
Frequently asked questions
How many devices does HEALTH CARE PRODUCTS, INC. have in the registry?
The registry currently lists 5 devices for HEALTH CARE PRODUCTS, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list HEALTH CARE PRODUCTS, INC.'s devices?
Among its 5 most recently registered devices, HEALTH CARE PRODUCTS, INC. has devices listed in FDA 510(k) (1 device) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do HEALTH CARE PRODUCTS, INC.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for HEALTH CARE PRODUCTS, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from HEALTH CARE PRODUCTS, INC. in the registry?
The most recently registered devices listed for HEALTH CARE PRODUCTS, INC. include Preference 11004, Preference 11002, Preference 11005 and Preference 11003.