ClearanceBrief
Company ยท US

Ria Diagnostics

FDA 510(k) clearances and medical device recalls filed under this name, 1978 to 1986. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
CDPRadioimmunoassay, Total Triiodothyronine1
CDXRadioimmunoassay, Total Thyroxine1
DDQAntigen, Antiserum, Control, Antithrombin Iii1
DONRadioimmunoassay, Digoxin (125-I), Rabbit Antibody, Solid Phase Sep.1
JLWRadioimmunoassay, Thyroid-Stimulating Hormone1
KHQRadioassay, Triiodothyronine Uptake1
LCARadioimmunoassay, Theophylline1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jan 24, 1986K855033T-3 UPTAKE/RIASSAY
Ria Diagnostics
KHQ
Jan 15, 1986K854798T-4 RIASSAY
Ria Diagnostics
CDX
Aug 12, 1985K852537T-3 RIASSAY
Ria Diagnostics
CDP
Feb 19, 1981K810296DIGOXIN RIA ASSAY
Ria Diagnostics
DON
Aug 27, 1980K801691TSH RIASSAY
Ria Diagnostics
JLW
Feb 25, 1980K792062THEOPHYLLINE RIASSAY
Ria Diagnostics
LCA
Jan 20, 1978K780012ANTITHROMBIN III RIA
Ria Diagnostics
DDQ

Latest recalls

DateFirm and productCodeLinked 510(k)
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