# Gelman Instrument Co.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 11 (1977–1978): 11 510(k) clearances
- Product codes: DAY (1), CJO (1), DDI (1), DBI (1), DFC (1), JQT (1), CZP (1), DAB (1), DFL (1), DEM (1), DEW (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
- K772075: Radial Immunodiffusion Kit-Complement (Feb 3, 1978)
- K772074: Radial Immunodiffusion Kit-Transferrin (Feb 3, 1978)
- K772073: Radial Immunodiffusion Kit-Comp. 3 (Feb 3, 1978)
- K772076: Radial Immunodiffusion Kit-Immunoglob. (Feb 3, 1978)
- K772078: Radial Immunodiffusion Kit-Haptoglobin (Feb 3, 1978)
- K772079: Radial Immunodiffusion Kit-Immunoglob.M (Feb 3, 1978)
- K772080: Radial Immunodiffusion Kit-Alph-L-Antit (Feb 3, 1978)
- K772077: Radial Immunodiffusion Kit-Immunoglob.G (Feb 3, 1978)

Source page: https://510kreport.com/company/gelman-instrument