# Coratomic, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 15 (1976–1986): 15 510(k) clearances
- Product codes: DXY (11), DTB (3)
- 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
- K863365: Modification of Sterility Cycle Parameters (Oct 8, 1986)
- K822791: Coratomic #VX5-105 & VX5-205 Pulse Gen. (Dec 15, 1982)
- K820939: C-101-P (Jun 22, 1982)
- K821033: Coratomic Model Ovalith-920 (May 28, 1982)
- K821014: Coratomic Model Ovalith 920BP (May 28, 1982)
- K810808: Coratomic Model Ovalith-920 (May 15, 1981)
- K802689: L-15T Endocardial Pacing Electrode (Oct 28, 1980)
- K800194: Ovalith P-BP Bipolar Cardiac Pacemaker (Feb 11, 1980)

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