Parexel Intl. Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
14
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K900385ACTA METRA/ACTA GNOSIS FIRMWARE PACKAGEJuly 9, 1991
K904902SMA 26 TRANSDUCERMarch 26, 1991
K904901L11, L12 LINEAR AND C11, C12 CONVEX ARRAY TRANSDUCMarch 26, 1991
K884800ACTA GENOS ELECTROCARDIOGRAPHJune 22, 1989
K862414FUJI CR IMAGING PLATEFebruary 26, 1987
K864519PHILIPS COMPUTED RADIOGRAPHY SYSTEM (PCR)February 13, 1987
K862415TYPE 633 COMPUTED RADIOGRAPHY (CR) FILMJuly 1, 1986
K862416FTI 100 MEDICAL THERMAL IMAGERJuly 1, 1986
K853295EMODREN EXCHANGEABLE PLASTIC BELLOWSAugust 20, 1985
K853296EMODREN GUIDE NEEDLE FOR DRAINAGE TUBE & EMODRENAugust 15, 1985
K851322PERSONAL C3 3-CHANNEL ELECTROCARDIOGRAPHMay 16, 1985
K842123PERSONAL CL SINGLE-CHANNEL ELECTROCARNovember 16, 1984
K842208NATURA-TONE OR LUXOPAL CL ACRYLICJuly 31, 1984
K841826NATURA-DENT VACUUM-FIRED PORCELAIN TEETHJuly 12, 1984