Phutex Products Co., Ltd.
IndonesiaFDA applicant, unverified
- Devices
- 1
What Phutex Products Co., Ltd. makes
Phutex Products Co., Ltd. manufactures patient examination gloves, designed for single-use in clinical settings to reduce cross-contamination during medical procedures.
The company’s portfolio is regulated under FDA 510(k) clearance as Class I devices and is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Patient Examination Glove Ref K890931
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Phutex Products Co., Ltd. have in the registry?
The registry currently lists 1 device for Phutex Products Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Phutex Products Co., Ltd.'s devices?
Among its 1 most recently registered device, Phutex Products Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Phutex Products Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Phutex Products Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Phutex Products Co., Ltd. in the registry?
The most recently registered devices listed for Phutex Products Co., Ltd. include PATIENT EXAMINATION GLOVE.