# Innotron of Oregon, Inc.

- Location (FDA's records): Portland, OR
- FDA decisions: 28 (1980–1990): 28 510(k) clearances
- Product codes: DLJ (10), LBZ (2), LGR (2), LEH (2), LFW (2), KLT (1), LGQ (1), LGS (1), KLQ (1), KHO (1), LCD (1), JJQ (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: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K903101: Innofluor (TM) Amikacin Calibrator Set (Aug 22, 1990)
- K903100: Innofluor (TM) Amikacin Reagent Set (Aug 9, 1990)
- K900707: Modified Accufluor Tobramycin Reagent & Calibrator (Apr 20, 1990)
- K900708: Modified Accufluor Vancomycin Reagent & Calibrator (Apr 19, 1990)
- K900705: Modified Accufluor Quinidine Reagent & Calibrator (Apr 12, 1990)
- K900704: Modified Accufluor Phenobarbital Reagent & Calibra (Apr 12, 1990)
- K900706: Modified Accufluor Theophylline Reagent & Calibra (Apr 12, 1990)
- K900703: Modified Accufluor Gentamicin Reagent & Calibrator (Apr 12, 1990)

Source page: https://510kreport.com/company/innotron-of-oregon