Paratex Product Co., Ltd.
ThailandFDA applicant, unverified
- Devices
- 1
What Paratex Product Co., Ltd. makes
Paratex Product Co., Ltd. manufactures patient examination gloves.
These gloves are classified as Class I medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Patient Examination Gloves Ref K893050
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Paratex Product Co., Ltd. have in the registry?
The registry currently lists 1 device for Paratex Product Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Paratex Product Co., Ltd.'s devices?
Among its 1 most recently registered device, Paratex Product Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Paratex Product Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Paratex Product Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Paratex Product Co., Ltd. in the registry?
The most recently registered devices listed for Paratex Product Co., Ltd. include PATIENT EXAMINATION GLOVES.