Medical Device Manufacturer · US , Mchenry , IL

Biorent Diagnostic, Inc. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 1981

Total

Cleared

Denied

Biorent Diagnostic, Inc. has 11 FDA 510(k) cleared chemistry devices. Based in Mchenry, US.

Historical record: 11 cleared submissions from 1981 to 1983.

Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.

Biorent Diagnostic, 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 - Biorent Diagnostic, Inc.

11 devices

1-11 of 11

OPTIMIZED UV-GOT REAGENT SET

K822493 · CIT

Chemistry · 34d

Cleared Sep 21, 1982

OPTIMIZED UV-GPT REAGENT SET

K822494 · CKA

Chemistry · 34d

Cleared Sep 17, 1982

OPTIMIZED UV-LDH REAGENT SET

K822492 · CFJ

Chemistry · 30d

Cleared Apr 14, 1982

COLORIMETRIC LDH REAGENT SET

K820768 · CFH

Chemistry · 23d

Cleared Mar 25, 1982

COLORIMETRIC URIC ACID REAGENT SET

K820632 · KNK

Chemistry · 17d

Cleared Jan 18, 1982

GLUCOSE ENZYME-COLOR REAGENT SET

K813555 · CGA

Chemistry · 27d

Cleared Dec 08, 1981

UV URIC ACID DETERMINATION

K813244 · CDO

Chemistry · 20d

Cleared Jul 10, 1981

CHOLESTEROL DETERMINATION

K811760 · CHH

Chemistry · 18d

Biorent Diagnostic, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Biorent Diagnostic, Inc.

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