# Latex Ind., Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 14 (1977–1981): 14 510(k) clearances
- Product codes: FCM (8), KOD (3), KNX (2), EYZ (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
- K812058: Akron Urinary Drainage Bat (Jul 31, 1981)
- K810281: Urological Catheters (Feb 25, 1981)
- K791674: Bladder Retention Catheterization Tray (Nov 5, 1979)
- K781751: Catheter, Akron Foley Teflon (Jan 22, 1979)
- K781433: Akron Male External Catheter (Nov 3, 1978)
- K772277: Bladder Retention-Cathetherizationtray (Mar 2, 1978)
- K772340: Catheterization Kit 732016-732018 (Feb 24, 1978)
- K780267: Cath Tray W/Out Catheter (Feb 24, 1978)

Source page: https://510kreport.com/company/latex-ind