# Parexel Intl. Corp.

- Location (FDA's records): Cambridge, MA
- FDA decisions: 14 (1984–1991): 14 510(k) clearances
- Product codes: ITX (2), DSI (2), DPS (2), GCY (1), ELL (1), IWZ (1), LLZ (1), LMC (1), BYY (1), EAM (1), ELM (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
- K900385: Acta Metra/Acta Gnosis Firmware Package (Jul 9, 1991)
- K904902: Sma 26 Transducer (Mar 26, 1991)
- K904901: L11, L12 Linear and C11, C12 Convex Array Transduc (Mar 26, 1991)
- K884800: Acta Genos Electrocardiograph (Jun 22, 1989)
- K862414: Fuji CR Imaging Plate (Feb 26, 1987)
- K864519: Philips Computed Radiography System (PCR) (Feb 13, 1987)
- K862415: Type 633 Computed Radiography (CR) Film (Jul 1, 1986)
- K862416: Fti 100 Medical Thermal Imager (Jul 1, 1986)

Source page: https://510kreport.com/company/parexel-intl