510(k) Report

FDA applicant

Alta Diagnostics, Inc.

Mchenry, IL5 decisions1979–19800 recalls

FDA records 5 decisions for Alta Diagnostics, Inc. (Mchenry, IL) from 1979 to 1980: 5 510(k) clearances. Most are in product codes JGJ (Photometric Method, Magnesium) and CET (Olive Oil Emulsion (Turbidimetric), Lipase). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, clinical chemistry panel, where it files most

How often FDA has decided Alta Diagnostics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Alta Diagnostics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Alta Diagnostics, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Alta Diagnostics, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Alta”

FDA records each applicant name separately; these may or may not be the same firm.