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

PTH-RIA

K Number: K844735 · Decision Apr 29, 1985
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
85
Applicant Total
31
Review Days
146

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Basic Information

Device Name
PTH-RIA
K Number
K844735
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1545
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Syncor Intl. Corp.
Date Received
December 4, 1984
Decision Date
April 29, 1985
Product Code
CEW
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
CEW Radioimmunoassay, Parathyroid Hormone

Similar 510(k) Clearances

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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
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. →