# Imm Enterprises, Ltd.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 52 (1983–1984): 52 510(k) clearances
- Product codes: HTD (14), KOA (4), GWZ (3), GES (3), GAD (2), BWB (2), EMF (2), HCZ (1), FZO (1), JYL (1), HOB (1), EMG (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
- K840311: Cat. 7-Ear, Nose & Throat Devices (May 9, 1984)
- K841387: Weston Rectal Snare (May 9, 1984)
- K841386: Kollmann Urethral Dilator (May 9, 1984)
- K840304: Category 17-Microbiology Devices (May 1, 1984)
- K840318: Cat. 14-Clinical Toxiology Devices (Apr 23, 1984)
- K840305: Category 1 Circulatory System Device (Apr 23, 1984)
- K840312: Cat. 8 Dental Devices (Apr 5, 1984)
- K834171: OP-Con Surg. Instrument #3 (Apr 4, 1984)

Source page: https://510kreport.com/company/imm-enterprises