Parexel Intl. Corp. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Parexel Intl. Corp. has 14 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 14 cleared submissions from 1984 to 1991. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Parexel Intl. Corp. Filter by specialty or product code using the sidebar.
14 devices
Cleared
Jul 09, 1991
ACTA METRA/ACTA GNOSIS FIRMWARE PACKAGE
Cardiovascular
526d
Cleared
Mar 26, 1991
L11, L12 LINEAR AND C11, C12 CONVEX ARRAY TRANSDUC
Radiology
147d
Cleared
Mar 26, 1991
SMA 26 TRANSDUCER
Radiology
147d
Cleared
Jun 22, 1989
ACTA GENOS ELECTROCARDIOGRAPH
Cardiovascular
218d
Cleared
Feb 26, 1987
FUJI CR IMAGING PLATE
Radiology
246d
Cleared
Feb 13, 1987
PHILIPS COMPUTED RADIOGRAPHY SYSTEM (PCR)
Radiology
88d
Cleared
Jul 01, 1986
TYPE 633 COMPUTED RADIOGRAPHY (CR) FILM
Radiology
6d
Cleared
Jul 01, 1986
FTI 100 MEDICAL THERMAL IMAGER
Radiology
6d
Cleared
Aug 20, 1985
EMODREN EXCHANGEABLE PLASTIC BELLOWS
General & Plastic Surgery
14d
Cleared
Aug 15, 1985
EMODREN GUIDE NEEDLE FOR DRAINAGE TUBE & EMODREN
General Hospital
9d
Cleared
May 16, 1985
PERSONAL C3 3-CHANNEL ELECTROCARDIOGRAPH
Cardiovascular
44d
Cleared
Nov 16, 1984
PERSONAL CL SINGLE-CHANNEL ELECTROCAR
Cardiovascular
171d
Cleared
Jul 31, 1984
NATURA-TONE OR LUXOPAL CL ACRYLIC
Dental
57d
Cleared
Jul 12, 1984
NATURA-DENT VACUUM-FIRED PORCELAIN TEETH
Dental
71d