Jiann FA Rubber Factory Co., Ltd.
TaiwanFDA applicant, unverified
- Devices
- 1
What Jiann FA Rubber Factory Co., Ltd. makes
Jiann FA Rubber Factory Co., Ltd. manufactures latex patient examination gloves, designed for single-use medical procedures requiring barrier protection.
These gloves are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Patient Examiaination Gloves (Latex) Ref K892247
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jiann FA Rubber Factory Co., Ltd. have in the registry?
The registry currently lists 1 device for Jiann FA Rubber Factory Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jiann FA Rubber Factory Co., Ltd.'s devices?
Among its 1 most recently registered device, Jiann FA Rubber Factory Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Jiann FA Rubber Factory Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Jiann FA Rubber Factory Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Jiann FA Rubber Factory Co., Ltd. in the registry?
The most recently registered devices listed for Jiann FA Rubber Factory Co., Ltd. include PATIENT EXAMIAINATION GLOVES (LATEX).