# The Urology Group

- Location (FDA's records): Mchenry, IL
- FDA decisions: 6 (1980–1984): 6 510(k) clearances
- Product codes: GEI (1), KNX (1), NAD (1), KQT (1), OCV (1), FZX (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
- K831703: Coverups (Jan 3, 1984)
- K831489: Surgical Tube Holder (Dec 12, 1983)
- K810739: Suction Wound Drainage Device (Jun 26, 1981)
- K810788: Surgical Tube Holder (Apr 17, 1981)
- K810787: Urologic Tube Holder (Mar 31, 1981)
- K801629: Cover-All Male Incontinence Device (Aug 12, 1980)

Source page: https://510kreport.com/company/urology-group