Medical Device Manufacturer · US , Mchenry , IL

Radioimmunoassay, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1978

Total

Cleared

Denied

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

Historical record: 9 cleared submissions from 1978 to 1980. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by Radioimmunoassay, Inc. Filter by specialty or product code using the sidebar.

Radioimmunoassay, Inc. 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 - Radioimmunoassay, Inc.

9 devices

1-9 of 9

Cleared Oct 10, 1980

TESTOSTERONE RADIOIMMUNOASSY KIT

K802135 · CDZ

Chemistry · 36d

Cleared Feb 13, 1980

LUTEINIZING HORMONE RADIOIMMUNOASSAY SYS

K800106 · CEP

Chemistry · 28d

Cleared Feb 13, 1980

FOLLICLE STIMULATING HORMONE

K800107 · CGJ

Chemistry · 28d

Cleared Jan 16, 1980

TRIIODOTHYRONINE RIA SYSTEM

K792539 · CDP

Chemistry · 37d

Cleared Nov 13, 1979

DIGOXIN RADIOIMMUNOASSAY SYSTEM

K792153 · DPB

Toxicology · 18d

Cleared Nov 13, 1979

THYROID STIMULATING HORMONE

K792154 · JLW

Chemistry · 19d

Cleared Oct 30, 1979

CORTISOL RADIOIMMUNOASSAY SYSTEM

K792036 · CGR

Chemistry · 19d

Cleared Jun 06, 1978

125 I-T3 UPTAKE REAGENT

Radioimmunoassay, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Radioimmunoassay, Inc.

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