# Medipart Jerry Alexander

- Location (FDA's records): Cary, IL
- FDA decisions: 49 (1984–1990): 49 510(k) clearances
- Product codes: IYT (23), CAH (8), BSJ (6), BYP (4), CCQ (2), CBL (1), BYX (1), BXJ (1), CBN (1), BTK (1), CAF (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
- K896885: Disposable Respirtory Kit (MP-200) (Feb 26, 1990)
- K896125: Medipart Disposable Xenon-133 Rebreathing MP-0133M (Feb 1, 1990)
- K896476: Disp. Radioaerosol Kit (MP-400-M) to Fit Shield (Jan 22, 1990)
- K896475: Disp. Radioaerosol Kit (MP-400) to Fit Lead Shield (Jan 22, 1990)
- K896124: Medipart Disposable Xenon-133 Rebreathing MP-0133 (Jan 22, 1990)
- K894138: Medipart Disposable Aerosol System MP-070-PTD (Sep 26, 1989)
- K893532: Resubmitted Radioaerosol Cont. System MP-963 (Aug 21, 1989)
- K862782: MP-XML Disposable Face Mask (Aug 1, 1986)

Source page: https://510kreport.com/company/medipart-jerry-alexander