FDA applicant

Accuimage Diagnostics Corp.

San Leandro, CA3 decisions1999–20030 recalls

FDA records 3 decisions for Accuimage Diagnostics Corp. (San Leandro, CA) from 1999 to 2003: 3 510(k) clearances. Most are in product codes JAK (System, X-Ray, Tomography, Computed) and LLZ (System, Image Processing, Radiological). Its devices cite 9 predicates, 1 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, radiology panel, where it files most

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

FDA decisions per year

No FDA decision for Accuimage Diagnostics Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Other applicant names beginning “Accuimage”

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

Accuimage, Inc. 1

Accuimage Diagnostics Corp.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Accuimage”