# Clinetics Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 9 (1980–1986): 9 510(k) clearances
- Product codes: CEP (2), CGJ (2), JZO (1), CKG (1), JHI (1), DGC (1), DHX (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
- K862180: Modified Cotropin Radioimmunoassay Kit (Jul 7, 1986)
- K844066: Cotropin Stimulataneous 57 CO-LH 125I I-FSH (Jan 18, 1985)
- K841580: TSH Receptor Antibody Kit 125I TSH (Oct 22, 1984)
- K833934: Adrenocorticotropic Hormone Test (Apr 4, 1984)
- K830357: Radioimmunoassay Immunoglobulins D.E (Mar 17, 1983)
- K823380: 125-I LH Radioimmunoassay Kit (Dec 22, 1982)
- K823379: 125-I FSH Radioimmunoassay Kit (Dec 22, 1982)
- K822152: HCG Beta Ria Kit (Sep 2, 1982)

Source page: https://510kreport.com/company/clinetics