Parexel Intl. Corp.
Parexel Intl. Corp. holds FDA 510(k) medical device clearances, first cleared 1984, most recent 1991.
Top product codes for Parexel Intl. Corp.
Recent clearances by Parexel Intl. Corp.
- K900385 — ACTA METRA/ACTA GNOSIS FIRMWARE PACKAGE
- K904901 — L11, L12 LINEAR AND C11, C12 CONVEX ARRAY TRANSDUC
- K904902 — SMA 26 TRANSDUCER
- K884800 — ACTA GENOS ELECTROCARDIOGRAPH
- K862414 — FUJI CR IMAGING PLATE
- K864519 — PHILIPS COMPUTED RADIOGRAPHY SYSTEM (PCR)
- K862415 — TYPE 633 COMPUTED RADIOGRAPHY (CR) FILM
- K862416 — FTI 100 MEDICAL THERMAL IMAGER
- K853295 — EMODREN EXCHANGEABLE PLASTIC BELLOWS
- K853296 — EMODREN GUIDE NEEDLE FOR DRAINAGE TUBE & EMODREN
- K851322 — PERSONAL C3 3-CHANNEL ELECTROCARDIOGRAPH
- K842123 — PERSONAL CL SINGLE-CHANNEL ELECTROCAR
- K842208 — NATURA-TONE OR LUXOPAL CL ACRYLIC
- K841826 — NATURA-DENT VACUUM-FIRED PORCELAIN TEETH
Data sourced from openFDA. This site is unofficial and independent of the FDA.