Aller/Guard, Inc.
Country not established
- Devices
- 1
What Aller/Guard, Inc. makes
Aller/Guard, Inc. manufactures the HMB AllergoGen skin prick test needle, a disposable device used for intradermal allergen testing to assess hypersensitivity reactions.
This product is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Hmb Allergogen Skin Prick Test Needle Ref K844221
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aller/Guard, Inc. have in the registry?
The registry currently lists 1 device for Aller/Guard, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aller/Guard, Inc.'s devices?
Among its 1 most recently registered device, Aller/Guard, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Aller/Guard, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Aller/Guard, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aller/Guard, Inc. in the registry?
The most recently registered devices listed for Aller/Guard, Inc. include HMB ALLERGOGEN SKIN PRICK TEST NEEDLE.