Gallimore Ent., Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Gallimore Ent., Inc. makes
Gallimore Ent., Inc. manufactures latex examination gloves, designed for medical and clinical examinations to ensure sterility and barrier protection during procedures.
These products are classified as Class I medical devices under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Latex Examination Glove Ref K904324
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gallimore Ent., Inc. have in the registry?
The registry currently lists 1 device for Gallimore Ent., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gallimore Ent., Inc.'s devices?
Among its 1 most recently registered device, Gallimore Ent., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Gallimore Ent., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Gallimore Ent., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Gallimore Ent., Inc. in the registry?
The most recently registered devices listed for Gallimore Ent., Inc. include LATEX EXAMINATION GLOVE.