Medical Device Manufacturer · US , Mchenry , IL

Clinetics Corp. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1980

Total

Cleared

Denied

Clinetics Corp. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 9 cleared submissions from 1980 to 1986. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by Clinetics Corp. Filter by specialty or product code using the sidebar.

Clinetics Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Clinetics Corp.

9 devices

1-9 of 9

Cleared Jul 07, 1986

MODIFIED COTROPIN RADIOIMMUNOASSAY KIT

K862180 · CEP

Chemistry · 28d

Cleared Jan 18, 1985

COTROPIN STIMULATANEOUS 57 CO-LH 125I I-FSH

K844066 · CGJ

Chemistry · 92d

Cleared Oct 22, 1984

TSH RECEPTOR ANTIBODY KIT 125I TSH

K841580 · JZO

Chemistry · 188d

Cleared Apr 04, 1984

ADRENOCORTICOTROPIC HORMONE TEST

K833934 · CKG

Chemistry · 142d

Cleared Mar 17, 1983

RADIOIMMUNOASSAY IMMUNOGLOBULINS D.E

K830357 · DGC

Chemistry · 42d

Cleared Dec 22, 1982

125-I FSH RADIOIMMUNOASSAY KIT

K823379 · CGJ

Chemistry · 40d

Cleared Dec 22, 1982

125-I LH RADIOIMMUNOASSAY KIT

Clinetics Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Clinetics Corp.

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