FDA applicant

Alamar Biosciences Laboratory, Inc.

Sacramento, CA26 decisions1989–19940 recalls

FDA records 26 decisions for Alamar Biosciences Laboratory, Inc. (Sacramento, CA) from 1989 to 1994: 26 510(k) clearances. Most are in product codes JWY (Manual Antimicrobial Susceptibility Test Systems) and LRG (Instrument For Auto Reader & Interpretation Of…). 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, microbiology panel, where it files most

How often FDA has decided Alamar Biosciences Laboratory, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Alamar Biosciences Laboratory, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Alamar Biosciences Laboratory, 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 “Alamar”

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

Alamar 7 Alamar Biosciences, Inc. 5

Alamar Biosciences Laboratory, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Alamar”