General Merchandise Co.
Hong Kong SAR ChinaFDA applicant, unverified
- Devices
- 1
What General Merchandise Co. makes
The company manufactures latex patient examination gloves designed for single-use medical procedures, ensuring barrier protection during clinical examinations.
These gloves are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer operates from the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K891857
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does General Merchandise Co. have in the registry?
The registry currently lists 1 device for General Merchandise Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list General Merchandise Co.'s devices?
Among its 1 most recently registered device, General Merchandise Co. has devices listed in FDA 510(k) (1 device).
What risk classes do General Merchandise Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for General Merchandise Co.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from General Merchandise Co. in the registry?
The most recently registered devices listed for General Merchandise Co. include PATIENT EXAMINATION GLOVES (LATEX).