Paramount Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Paramount Products, Inc. makes
Paramount Products, Inc. manufactures non-sterile masks and caps, as well as patient examination gloves.
The company's devices are classified as Class I and Class II and are listed in the FDA 510(k) registry. Paramount Products, Inc. is based in the US.
Catalogue
Non-Sterile Masks And Caps Ref K892118
Regimes: 510(k) Registry: 510(k)Patient Examination Glove Ref K891017
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Paramount Products, Inc. have in the registry?
The registry currently lists 2 devices for Paramount Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Paramount Products, Inc.'s devices?
Among its 2 most recently registered devices, Paramount Products, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Paramount Products, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Paramount Products, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Paramount Products, Inc. in the registry?
The most recently registered devices listed for Paramount Products, Inc. include NON-STERILE MASKS AND CAPS and PATIENT EXAMINATION GLOVE.