Ampac Rubber Co., Ltd.
TaiwanFDA applicant, unverified
- Devices
- 1
What Ampac Rubber Co., Ltd. makes
Ampac Rubber Co., Ltd. manufactures patient examination gloves made from latex, designed for single-use medical procedures and examinations.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K892511
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ampac Rubber Co., Ltd. have in the registry?
The registry currently lists 1 device for Ampac Rubber Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ampac Rubber Co., Ltd.'s devices?
Among its 1 most recently registered device, Ampac Rubber Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Ampac Rubber Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ampac Rubber Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ampac Rubber Co., Ltd. in the registry?
The most recently registered devices listed for Ampac Rubber Co., Ltd. include PATIENT EXAMINATION GLOVES (LATEX).