# Pennwalt Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 6 (1978–1983): 6 510(k) clearances
- Product codes: EAP (2), EJK (1), EHD (1), EBC (1), BXX (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
- K833241: Intrex (Oct 28, 1983)
- K801860: S.S. White-Pennwalt Renew Calcium Hydrox (Oct 10, 1980)
- K801274: S.S. White-Pennwalt Prelude Pit Sealant (Jun 9, 1980)
- K800063: XR-710 (Mar 3, 1980)
- K800133: Panorex II Dental X-Ray Unit (Mar 3, 1980)
- K780981: Portable Pneumatic Calibrator 65-150 (Aug 2, 1978)

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