# Linton Biomed Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 5 (1982–1984): 5 510(k) clearances
- Product codes: DRS (3), FPA (2)
- 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
- K841772: Heparin Cap, Injection Cap Male Luer- (Jul 6, 1984)
- K831348: Fluid Admin. Set Afs-1C (May 27, 1983)
- K820202: Continuous Flush Device/Fdi (Feb 12, 1982)
- K820201: Dispos. Monitoring Sys/LI ET AL (Feb 12, 1982)
- K820203: Fluid Administrative Set, Afi (Feb 5, 1982)

Source page: https://510kreport.com/company/linton-biomed