FDA applicant

Squibb Diagnostics

New Brunswick, NJ3 decisions1983–19890 recalls

FDA records 3 decisions for Squibb Diagnostics (New Brunswick, NJ) from 1983 to 1989: 3 510(k) clearances. Most are in product codes FRN (Pump, Infusion) and HAM (Apparatus, Electrosurgical). 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Squibb Diagnostics since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Squibb Diagnostics’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 “Squibb”

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

Squibb & Sons, Inc. 5 Squibb-Novo, Inc. 2

Squibb Diagnostics

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Squibb”