# Syncor Intl. Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 31 (1983–1995): 31 510(k) clearances
- Product codes: JHI (4), KXK (3), LJP (2), CEP (2), CGJ (2), CKG (2), IWA (2), JAQ (1), CEW (1), CDP (1), MOT (1), CDX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K945825: Secure Safety Insert (Apr 10, 1995)
- K851828: Irradiator for Biological Materials Ibl-437-C (Sep 19, 1985)
- K850433: Cesium 137 Endometrial Source (Aug 21, 1985)
- K852023: Cesium 137 Source, CSM-4, CSM-11, CSM-41 (Aug 21, 1985)
- K852665: Syncor Trich Direct Immunofluorescence Assay (Aug 13, 1985)
- K851033: Syncortech Chlamydia Direct Speciman Kit (Jun 21, 1985)
- K844735: PTH-Ria (Apr 29, 1985)
- K850726: Wire Cutters, Brachytherapy-Table Top & Hand Held (Mar 26, 1985)

Source page: https://510kreport.com/company/syncor-intl