# Exitec, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 4 (1982–1983): 4 510(k) clearances
- Product codes: HIB (2), KNT (1), FER (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
- K822085: Pro-Scope (May 9, 1983)
- K822087: Dia Scope (Nov 17, 1982)
- K822086: Dia-Spec (Nov 8, 1982)
- K822084: Pro-Spec (Aug 19, 1982)

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