Medical Device Manufacturer · US , Mchenry , IL

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

31 submissions · 31 cleared · Since 1983

Total

Cleared

Denied

Syncor Intl. Corp. has 31 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 31 cleared submissions from 1983 to 1995. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by Syncor Intl. Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Syncor Intl. Corp.

31 devices

1-12 of 31

Cleared Apr 10, 1995

SECURE SAFETY INSERT

K945825 · FMI

General Hospital · 132d

Cleared Sep 19, 1985

IRRADIATOR FOR BIOLOGICAL MATERIALS IBL-437-C

K851828 · MOT

Radiology · 146d

Cleared Aug 21, 1985

CESIUM 137 ENDOMETRIAL SOURCE

K850433 · KXK

Radiology · 198d

Cleared Aug 21, 1985

CESIUM 137 SOURCE, CSM-4, CSM-11, CSM-41

K852023 · KXK

Radiology · 105d

Cleared Aug 13, 1985

SYNCOR TRICH DIRECT IMMUNOFLUORESCENCE ASSAY

K852665 · JWZ

Microbiology · 50d

Cleared Jun 21, 1985

SYNCORTECH CHLAMYDIA DIRECT SPECIMAN KIT

FLOOD SOURCES & DOSE CALIBRATORS W/VARIOUS NUCLIDS

WIRE CUTTERS, BRACHYTHERAPY-TABLE TOP & HAND HELD

K850726 · IWA

Radiology · 32d

Cleared Mar 01, 1985

PENPOINT, FLEXIBLE & SPOT MARKERS & RADOACTIVE RUL

K850207

Radiology · 42d

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

FDA 510(k) cleared devices by Syncor Intl. Corp.

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