Ap Intl., Inc.
Country not established
- Devices
- 1
What Ap Intl., Inc. makes
Ap Intl., Inc. manufactures latex patient examination gloves designed for clinical use, providing barrier protection during medical procedures.
These gloves are classified as Class I devices under FDA regulations and are recorded in the 510(k) clearance database. The company is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K891546
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ap Intl., Inc. have in the registry?
The registry currently lists 1 device for Ap Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ap Intl., Inc.'s devices?
Among its 1 most recently registered device, Ap Intl., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Ap Intl., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ap Intl., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ap Intl., Inc. in the registry?
The most recently registered devices listed for Ap Intl., Inc. include PATIENT EXAMINATION GLOVES (LATEX).