Data / Medical devices / United States / Alta Diagnostics, Inc.
Alta Diagnostics, Inc.: FDA-registered device maker in Carson City, NV, United States, 1 510(k) clearance
Alta Diagnostics, Inc. is registered with the FDA (registration 2084170) in Carson City, NV, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 9, 1989. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2084170
- Address
- 3123 Research Way Ste 214, Carson City, NV, United States, 89706
- Owner or operator
- ALTA DIAGNOSTICS, INC. (9000337)
- Roles
- Repackager or relabeler
- First device listed
- February 11, 2008
- Registered through
- 2026
- Brand names listed
- Alta Diagnostics Urine Dipstick Control
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Urinalysis Controls (Assayed And Unassayed) | JJW | 1 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| March 9, 1989 | K890577 | KENLOR LIQUID URINE CONTROL | JJW | Substantially Equivalent | Kenlor Industries, Inc. | accessdata.fda.gov |
Compare with other makers
Updated March 9, 1989. 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.