510(k) Report

FDA applicant

Analytical Luminescence Laboratory, Inc.

San Diego, CA2 decisions1983–19850 recalls

FDA records 2 decisions for Analytical Luminescence Laboratory, Inc. (San Diego, CA) from 1983 to 1985: 2 510(k) clearances. Most are in product codes LIO (Device, Specimen Collection) and JXA (Kit, Screening, Urine). 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 Analytical Luminescence Laboratory, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Analytical Luminescence Laboratory, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • LIODevice, Specimen Collection1decision
  • JXAKit, Screening, Urine1decision

What has FDA decided for it lately?

  • K851387Microstatic Urine Transport Tube for C & SAnalytical Luminescence Laboratory, Inc. · 1985
  • K820126Rapid Bacteriuria Screening TestAnalytical Luminescence Laboratory, Inc. · 1983

All 2 as Analytical Luminescence Laboratory, Inc. →

Other applicant names beginning “Analytical”

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

Analytical Products, Inc. 59Analytical Control Systems, Inc. 42Analytical & Research Chemicals, Inc. 12Analytical Industries, Inc. 3Analytical Development Assoc. Corp. 1