Procare Industrial Co., Limited
ChinaFDA applicant, unverified FDA FEI 3009449769
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Procare Industrial Co., Limited makes
Procare Industrial Co., Limited manufactures the Allerhope Allergy Skin Tester, a device designed for intradermal allergy testing to identify skin sensitivities.
The Allerhope Allergy Skin Tester is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Allerhope Allergy Skin Tester Ref K162917
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3009449769
- Address
- Science Avenue 9, Hi-Tech Zone, ZHENGZHOU Henan
Frequently asked questions
How many devices does Procare Industrial Co., Limited have in the registry?
The registry currently lists 1 device for Procare Industrial Co., Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Procare Industrial Co., Limited's devices?
Among its 1 most recently registered device, Procare Industrial Co., Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Procare Industrial Co., Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Procare Industrial Co., Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Procare Industrial Co., Limited in the registry?
The most recently registered devices listed for Procare Industrial Co., Limited include Allerhope Allergy Skin Tester.