Data / Medical devices / China / Procare Industrial Co., Limited
Procare Industrial Co., Limited: FDA-registered device maker in ZHENGZHOU Henan, China, 1 510(k) clearance
Procare Industrial Co., Limited is registered with the FDA (registration 3009449769) in ZHENGZHOU Henan, China. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 17, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009449769
- Address
- Science Avenue 9, Hi-Tech Zone, ZHENGZHOU Henan, China, 450000
- Owner or operator
- PROCARE INDUSTRIAL CO., LIMITED (10038360)
- Roles
- Manufacturer
- First device listed
- October 8, 2011
- Registered through
- 2026
- Brand names listed
- Allerhope Allergy Skin Tester
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Allergen And Vaccine Delivery Needles | SCL | 2 | Manufacturer | accessdata.fda.gov |
| Applicator, Absorbent Tipped, Non-Sterile | KXF | 1 | Manufacturer | accessdata.fda.gov |
| Applicator, Absorbent Tipped, Sterile | KXG | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 17, 2017 | K162917 | Allerhope Allergy Skin Tester | SCL | Substantially Equivalent | Procare Industrial Co., Limited | accessdata.fda.gov |
Compare with other makers
- All makers of Allergen And Vaccine Delivery Needles
- All makers of Applicator, Absorbent Tipped, Sterile
- All makers of Applicator, Absorbent Tipped, Non-Sterile
Updated August 17, 2017. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.