510(k) Report

FDA applicant

Specific Diagnostics, LLC

San Jose, CA1 decision2024–20240 recalls

FDA records 1 decision for Specific Diagnostics, LLC (San Jose, CA) in 2024: 1 510(k) clearance. All are in product code SAN (Automated Antimicrobial Susceptibility Test…). Its devices cite 1 predicate, 0 of them its own earlier devices. 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 Specific Diagnostics, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2024: 1
2024high 1 (2024) · low 0 (2025)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2024.

FIG. 1 — Specific Diagnostics, LLC by year, 2024–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • SANAutomated Antimicrobial Susceptibility Test System For Positive Blood Culture Samples1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K230675VITEK REVEAL GN AST Assay and VITEK REVEAL AST SystemSpecific Diagnostics, LLC · 20241cites it

What has FDA decided for it lately?

  • K230675VITEK REVEAL GN AST Assay and VITEK REVEAL AST SystemSpecific Diagnostics, LLC · 2024

The one decision as Specific Diagnostics, LLC →