# Becton Dickinson Advanced Diagnostics

- Location (FDA's records): Sparks, MD
- FDA decisions: 10 (1991–1994): 10 510(k) clearances
- Product codes: JHI (3), JJE (1), JLW (1), GTZ (1), KHQ (1), CDX (1), JJY (1), GTY (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
- K935667: Qtest (R) Strep (Apr 21, 1994)
- K931294: IQ Tuptake Assay (Jul 22, 1993)
- K931295: IQ TT4 Assay (Jul 20, 1993)
- K926356: Precise (TM) HCG (Urine/Serum) and Prcise (TM) Preg (Mar 18, 1993)
- K925132: Becton Dickinson Thyroid Stimulating Hormone Syste (Dec 28, 1992)
- K923673: Precise Strep a (Sep 28, 1992)
- K923060: IQ Immunochemistry Sistem; IQ TSH Assay (Sep 15, 1992)
- K914958: Riatrac Plus (Mar 18, 1992)

Source page: https://510kreport.com/company/becton-dickinson-advanced-diagnostics