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.

Syncor Intl. Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

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