ClearanceBrief
Company ยท US

Clinical Diagnostics, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1977 to 1998. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
CGAGlucose Oxidase, Glucose3
CDXRadioimmunoassay, Total Thyroxine1
CEMElectrode, Ion Specific, Potassium1
CGRRadioimmunoassay, Cortisol1
JJGAnalyzer, Chemistry, Centrifugal, For Clinical Use1
LQDRecorder, Attention Task Performance1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jan 2, 1998K971653GLUCOCHEK POCKETLAB II BLOOD GLUCOSE SYSTEM
Clinical Diagnostics, Inc.
CGA
Feb 22, 1996K951457GLUCOCHEK POCKETLAB
Clinical Diagnostics, Inc.
CGA
Jan 17, 1995K940215GLUCOCHEK
Clinical Diagnostics, Inc.
CGA
Jun 2, 1986K854903GORDON DIAGNOSTIC SYSTEM MODEL I
Clinical Diagnostics, Inc.
LQD
Oct 25, 1977K771813CENTRIFICHEM SYS 400 ANALYZER
Clinical Diagnostics, Inc.
JJG
Jul 11, 1977K771118CENTRIA SEPARATION COLUMNS TYPE A
Clinical Diagnostics, Inc.
CEM
Jun 23, 1977K771117CENTRIA CORTISOL RIA
Clinical Diagnostics, Inc.
CGR
Mar 16, 1977K761272CENTRIA T4 RIA
Clinical Diagnostics, Inc.
CDX

Latest recalls

DateFirm and productCodeLinked 510(k)
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