Jann Maw (U.S.A.), Inc.
Country not established
- Devices
- 1
What Jann Maw (U.S.A.), Inc. makes
Jann Maw (U.S.A.), Inc. manufactures patient examination gloves, designed for clinical use in medical settings to ensure hygiene and protection during procedures.
The company’s products are classified as Class I devices under U.S. regulations and are listed via the FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
J.M. Patient Examination Gloves Ref K891624
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jann Maw (U.S.A.), Inc. have in the registry?
The registry currently lists 1 device for Jann Maw (U.S.A.), Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jann Maw (U.S.A.), Inc.'s devices?
Among its 1 most recently registered device, Jann Maw (U.S.A.), Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Jann Maw (U.S.A.), Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Jann Maw (U.S.A.), Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Jann Maw (U.S.A.), Inc. in the registry?
The most recently registered devices listed for Jann Maw (U.S.A.), Inc. include J.M. PATIENT EXAMINATION GLOVES.