Alta Diagnostics, Inc.
Carson City, NV, US
ALTA DIAGNOSTICS, INC. appears in FDA device records in Carson City, NV. FDA records list 5 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 5 510(k) clearances for Alta Diagnostics, Inc. between 1979 and 1980. The busiest year on record is 1979, with 3. The most recent is 1980, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1979 | 3 |
| 1980 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K800327 | MAGNESIUM REAGENT | JGJ | Substantially Equivalent | |
| K792545 | URIC ACID KIT | KNK | Substantially Equivalent | |
| K792546 | FETAL CHECK | KJR | Substantially Equivalent | |
| K790797 | AMYLASE REAGENT SET | KHM | Substantially Equivalent | |
| K790796 | LIPASE REAGENT SET | CET | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 2084170 | 2084170 | ALTA DIAGNOSTICS, INC. | 3123 Research Way Ste 214, Carson City, NV 89706 US | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain