# Culture Kits, Inc.

- Location (FDA's records): Norwich, NY
- FDA decisions: 9 (1985–1991): 9 510(k) clearances
- Product codes: JSI (3), JTZ (2), JSG (1), JXA (1), JSX (1), JSJ (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
- K911846: Uri-Three (TM), Modification (Oct 4, 1991)
- K854672: Candi-Kit TM (Jul 11, 1986)
- K853488: Staph Kit (Aug 28, 1985)
- K851225: Urine Duo (Aug 13, 1985)
- K852582: Goni-Kit (Jul 12, 1985)
- K852480: Derm-Kit (Jul 9, 1985)
- K851518: Mueller Hinton Sensitivity Plate (Apr 29, 1985)
- K850765: Strep-Kit (Apr 24, 1985)

Source page: https://510kreport.com/company/culture-kits