# Cutter Laboratories, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 39 (1976–1986): 39 510(k) clearances
- Product codes: ELW (5), CAH (3), EMA (2), ITG (2), KXZ (1), EFB (1), GAA (1), IQI (1), EJL (1), HWE (1), FOZ (1), EBH (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
- K861315: Hyperbaric Penetration Extension Set (May 21, 1986)
- K854106: Baysilex (Mar 17, 1986)
- K842324: Perfourm (Nov 9, 1984)
- K834106: Intravenous Infusion Controller (May 30, 1984)
- K832237: Orthopedic Casting Tape Maxcast (Aug 16, 1983)
- K823214: Dosimetric Release Program - Admin. Set (Jan 12, 1983)
- K821326: Cutter Bond Polycarboxylate Cement (May 28, 1982)
- K813532: Cutterbond Zinc Phosphate Cement (Mar 2, 1982)

Source page: https://510kreport.com/company/cutter-laboratories