# Ind Diagnostic, Inc.

- Location (FDA's records): Delta, B.C., CA
- FDA decisions: 8 (2003–2012): 8 510(k) clearances
- Product codes: JHI (2), CGJ (1), JIL (1), LCX (1), DKZ (1), KHE (1), NGJ (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: 5 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K103037: Ind Urinary Tract Infection (Uti) Test Strips (Apr 17, 2012)
- K100031: Ind One Step Fecal Occult Blood Test Model 440-10 (Jul 19, 2010)
- K063390: Urine Chemistry Analyzer UR-50 (Mar 1, 2007)
- K060810: One Step Drug Test - Amp/Met/Mor/THC/Coc (Aug 7, 2006)
- K052694: One Step HCG Pregnancy Test - 2000 Miu/ML, Model 100 Series. (Dec 16, 2005)
- K052662: One Step FSH Menopausal Test (Nov 30, 2005)
- K050741: Ind One Step HCG Pregnancy Test - Cassette Format (May 16, 2005)
- K023638: Cassette/Urine HCG (Jan 3, 2003)

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