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

CURIETRON

K Number: K840127 · Decision Mar 19, 1984
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
206
Applicant Total
31
Review Days
68

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Basic Information

Device Name
CURIETRON
K Number
K840127
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5700
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Syncor Intl. Corp.
Date Received
January 11, 1984
Decision Date
March 19, 1984
Product Code
JAQ
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
JAQ System, Applicator, Radionuclide, Remote-Controlled

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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
K850433 CESIUM 137 ENDOMETRIAL SOURCE
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
Search all 31 clearances from Syncor Intl. Corp. →