Charlton Assoc.
Country not established
- Devices
- 2
What Charlton Assoc. makes
Charlton Assoc. manufactures pregnancy tests, including the BIONIKE A/Q Pregnancy Test and the BODYWISE Pregnancy Test.
The company's devices are classified as Class II and listed in the FDA 510(k) registry. Charlton Assoc. is based in the US.
Catalogue
Bionike A/Q Pregnancy Test Ref K951136
Regimes: 510(k) Registry: 510(k)Bodywise Pregnancey Test Ref K941771
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Charlton Assoc. have in the registry?
The registry currently lists 2 devices for Charlton Assoc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Charlton Assoc.'s devices?
Among its 2 most recently registered devices, Charlton Assoc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Charlton Assoc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Charlton Assoc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Charlton Assoc. in the registry?
The most recently registered devices listed for Charlton Assoc. include BIONIKE A/Q PREGNANCY TEST and BODYWISE PREGNANCEY TEST.