Medical Device Manufacturer · US , Mchenry , IL

Parexel Intl. Corp. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1984

Total

Cleared

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.

FDA 510(k) Regulatory Record - Parexel Intl. Corp.

14 devices

1-12 of 14

Cleared Jul 09, 1991

ACTA METRA/ACTA GNOSIS FIRMWARE PACKAGE

K900385 · DSI

Cardiovascular · 526d

Cleared Mar 26, 1991

L11, L12 LINEAR AND C11, C12 CONVEX ARRAY TRANSDUC

ACTA GENOS ELECTROCARDIOGRAPH

K884800 · DPS

Cardiovascular · 218d

Cleared Feb 26, 1987

FUJI CR IMAGING PLATE

K862414 · EAM

Radiology · 246d

Cleared Feb 13, 1987

PHILIPS COMPUTED RADIOGRAPHY SYSTEM (PCR)

K864519 · LLZ

Radiology · 88d

Cleared Jul 01, 1986

TYPE 633 COMPUTED RADIOGRAPHY (CR) FILM

K862415 · IWZ

Radiology · 6d

Cleared Jul 01, 1986

FTI 100 MEDICAL THERMAL IMAGER

K862416 · LMC

Radiology · 6d

Cleared Aug 20, 1985

EMODREN EXCHANGEABLE PLASTIC BELLOWS

K853295 · GCY

General & Plastic Surgery · 14d

Cleared Aug 15, 1985

EMODREN GUIDE NEEDLE FOR DRAINAGE TUBE & EMODREN

K853296 · BYY

General Hospital · 9d

Cleared May 16, 1985

PERSONAL C3 3-CHANNEL ELECTROCARDIOGRAPH

K851322 · DPS

Cardiovascular · 44d

Cleared Nov 16, 1984

PERSONAL CL SINGLE-CHANNEL ELECTROCAR

K842123 · DSI

Cardiovascular · 171d

Parexel Intl. Corp. - FDA 510(k) Cleared Devices

Filters