# Old Delft Corp. of America

- Location (FDA's records): Fairfax, VA
- FDA decisions: 3 (1986–1986): 3 510(k) clearances
- Product codes: KPR (1), KPZ (1), JAD (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
- K862616: Amber-Chest (Sep 2, 1986)
- K861431: Therapax HT 150T (May 21, 1986)
- K854410: Veriflex (Feb 12, 1986)

Source page: https://510kreport.com/company/old-delft-of-america