Asia Way Trading, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Asia Way Trading, Inc. makes
Asia Way Trading, Inc. manufactures sterile and non-sterile patient examination gloves made from latex, designed for clinical and medical use.
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
Sterile Patient Examination Gloves (Latex) Ref K893095
Regimes: 510(k) Registry: 510(k)Non-Sterile Patient Examination Gloves (Latex) Ref K892747
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Asia Way Trading, Inc. have in the registry?
The registry currently lists 2 devices for Asia Way Trading, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Asia Way Trading, Inc.'s devices?
Among its 2 most recently registered devices, Asia Way Trading, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Asia Way Trading, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Asia Way Trading, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Asia Way Trading, Inc. in the registry?
The most recently registered devices listed for Asia Way Trading, Inc. include STERILE PATIENT EXAMINATION GLOVES (LATEX) and NON-STERILE PATIENT EXAMINATION GLOVES (LATEX).