FDA applicant

Vanguard Diagnostic Systems

La Habra, CA2 decisions1987–19870 recalls

FDA records 2 decisions for Vanguard Diagnostic Systems (La Habra, CA) in 1987: 2 510(k) clearances. All are in product code JJY (Multi-Analyte Controls, All Kinds (Assayed)). 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 Vanguard Diagnostic Systems’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vanguard Diagnostic Systems since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Vanguard”

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

Vanguard Medical Concepts, Inc. 33 Vanguard Biomedical Corp. 10 Vanguard Container Corp. 1

Vanguard Diagnostic Systems

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Vanguard”