Montrose Intl., Corp.
Country not established
- Devices
- 1
What Montrose Intl., Corp. makes
Montrose Intl., Corp. manufactures patient examination gloves made from latex.
The company is based in the United States, and its product is classified as a Class I medical device listed in the FDA 510(k) registry.
Catalogue
Patient Examination Glove (Latex) Ref K891980
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Montrose Intl., Corp. have in the registry?
The registry currently lists 1 device for Montrose Intl., Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Montrose Intl., Corp.'s devices?
Among its 1 most recently registered device, Montrose Intl., Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Montrose Intl., Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Montrose Intl., Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Montrose Intl., Corp. in the registry?
The most recently registered devices listed for Montrose Intl., Corp. include PATIENT EXAMINATION GLOVE (LATEX).