FDA applicant

Accu Science Corp.

Anaheim, CA2 decisions1987–19870 recalls

FDA records 2 decisions for Accu Science Corp. (Anaheim, CA) in 1987: 2 510(k) clearances. All are in product code GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). 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, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for Accu Science Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Accu Science 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 “Accu”

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

Accu-Line 4 Accu-Stat Diagnostics, Inc. 3 Accu-Med Corp. 1 Accu-Speed, Incorporated 1 Accu-Path 1

Accu Science Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Accu”