Garrett-Hewitt Intl., Inc.
Country not established
- Devices
- 1
What Garrett-Hewitt Intl., Inc. makes
Garrett-Hewitt Intl., Inc. manufactures latex patient examination gloves, designed for clinical use in medical examinations and procedures.
These products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K891177
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Garrett-Hewitt Intl., Inc. have in the registry?
The registry currently lists 1 device for Garrett-Hewitt Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Garrett-Hewitt Intl., Inc.'s devices?
Among its 1 most recently registered device, Garrett-Hewitt Intl., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Garrett-Hewitt Intl., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Garrett-Hewitt Intl., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Garrett-Hewitt Intl., Inc. in the registry?
The most recently registered devices listed for Garrett-Hewitt Intl., Inc. include PATIENT EXAMINATION GLOVES (LATEX).