Perfekta Intl., Ltd.
Hong Kong SAR ChinaFDA applicant, unverified
- Devices
- 1
What Perfekta Intl., Ltd. makes
Perfekta Intl., Ltd. manufactures DuraPro patient examination gloves, designed for single-use clinical procedures requiring barrier protection.
These gloves are classified as Class I devices under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Durapro (Patient Examination Gloves) Ref K892130
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Perfekta Intl., Ltd. have in the registry?
The registry currently lists 1 device for Perfekta Intl., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Perfekta Intl., Ltd.'s devices?
Among its 1 most recently registered device, Perfekta Intl., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Perfekta Intl., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Perfekta Intl., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Perfekta Intl., Ltd. in the registry?
The most recently registered devices listed for Perfekta Intl., Ltd. include DURAPRO (PATIENT EXAMINATION GLOVES).