# Ameritek, Inc.

- Location (FDA's records): Seattle, WA
- FDA decisions: 17 (1986–2000): 17 510(k) clearances
- Product codes: JHI (2), DKZ (2), KYG (1), KHE (1), DJG (1), CEP (1), JIL (1), DIO (1), HNH (1), HPN (1), HKX (1), LDJ (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
- K001215: Dbest HCG 2 IU/ML Test Kit (Jun 22, 2000)
- K990873: Dbest Urinary Tract Infection Test Kit for Home-Use (Sep 1, 1999)
- K990681: Dbset Multidrug Screen Test Kit (Jul 15, 1999)
- K984269: Dbest Occult Blood Test Kit (May 11, 1999)
- K983190: Dbest Opiates Test Kit (Nov 18, 1998)
- K983191: Dbest Cocaine Test Kit (Nov 18, 1998)
- K983188: Dbest Tetrahydrocannabinol Test Kit (Nov 18, 1998)
- K983189: Dbest Methamphetamines Test Kit (Nov 18, 1998)

Source page: https://510kreport.com/company/ameritek