# Kent Laboratories, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 40 (1977–1995): 40 510(k) clearances
- Product codes: DEW (5), DFK (3), DDB (3), MSJ (2), DFZ (2), JZJ (2), DAS (2), CZX (1), DFH (1), DCN (1), DBA (1), DAD (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
- K951966: Human Prealbumin Radial Immunodiffusion Kit (Jun 1, 1995)
- K951967: Human C1 Inactivator or C-1 Esterase Inhibitor Radial Immunodiffusion Kit (May 30, 1995)
- K951968: Human C1Q Radial Immunodiffusion Kit (May 30, 1995)
- K950102: Human C-5 Radial Immunodiffusion Kit (Apr 10, 1995)
- K850683: 72 Determ. Size Radial Immunodiffusion Test ALPHA2 (Nov 27, 1985)
- K850682: 72 Determ. Size Radial Immuno. Test Human Cerulopl (Nov 25, 1985)
- K850691: Antiserum to Human Apolipoprotein a-I (Nov 1, 1985)
- K850686: Antiserum to Human Prealbumin (Nov 1, 1985)

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