FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CESIUM 137 ENDOMETRIAL SOURCE

K Number: K850433 · Decision Aug 21, 1985
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
150
Applicant Total
31
Review Days
198

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Basic Information

Device Name
CESIUM 137 ENDOMETRIAL SOURCE
K Number
K850433
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5730
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Syncor Intl. Corp.
Date Received
February 4, 1985
Decision Date
August 21, 1985
Product Code
KXK
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KXK Source, Brachytherapy, Radionuclide

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KXK), ordered by most recent decision date.

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Other Clearances by Syncor Intl. Corp.

K Number Device Name
K945825 SECURE SAFETY INSERT
K851828 IRRADIATOR FOR BIOLOGICAL MATERIALS IBL-437-C
K852023 CESIUM 137 SOURCE, CSM-4, CSM-11, CSM-41
K852665 SYNCOR TRICH DIRECT IMMUNOFLUORESCENCE ASSAY
K851033 SYNCORTECH CHLAMYDIA DIRECT SPECIMAN KIT
K844735 PTH-RIA
K850163 IRIDIUM 192 WIRES
K850208 FLOOD SOURCES & DOSE CALIBRATORS W/VARIOUS NUCLIDS
K850726 WIRE CUTTERS, BRACHYTHERAPY-TABLE TOP & HAND HELD
K850434 CS137 SEALED SOURCES
Search all 31 clearances from Syncor Intl. Corp. →