FDA applicant

Syncor Intl. Corp.

Mchenry, IL31 decisions1983–19950 recalls

FDA records 31 decisions for Syncor Intl. Corp. (Mchenry, IL) from 1983 to 1995: 31 510(k) clearances. Most are in product codes JHI (Visual, Pregnancy Hcg, Prescription Use) and KXK (Source, Brachytherapy, Radionuclide). 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 Syncor Intl. Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Syncor Intl. Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Syncor”

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

Syncor Pharmaceuticals, Inc. 4 Syncor International, Inc. 2 Syncor Radiation Management 1

Syncor Intl. Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Syncor”