Medical Device Manufacturer · US , Walker , MI

Bioclinical Group - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1982

Total

Cleared

Denied

Bioclinical Group has 9 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 9 cleared submissions from 1982 to 1986. Primary specialty: Chemistry.

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

Bioclinical Group 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 - Bioclinical Group

9 devices

1-9 of 9

Cleared Sep 25, 1986

FREE T3 RADIOIMMUNOASSAY KIT

K862968 · KHQ

Chemistry · 50d

Cleared Oct 16, 1985

LH/FSH RADIOIMMUNOASSAY KIT

K853837 · CEP

Chemistry · 30d

Cleared Sep 12, 1983

CORTISOL RADIOIMMUNOASSAY KIT

K832638 · CGR

Chemistry · 39d

Cleared Dec 15, 1982

BIO MAG FREE T4 RADIOIMMUNOASSAY KIT

K823005 · CEC

Chemistry · 64d

Cleared Nov 05, 1982

BIO MAG TOTAL T4 RADIOIMMUNOASSAY KIT

K823004 · CDX

Chemistry · 24d

Cleared Oct 27, 1982

RADIOIMMUNOASSAY, HUMAN CHORRIONIC

K822840 · JHI

Chemistry · 34d

Cleared Sep 14, 1982

B-HCG RADIOIMMUNOASSAY KIT

K822515 · JHI

Chemistry · 25d

Cleared Jun 01, 1982

FREE T4 RADIOIMMUNOASSAY KIT

K821241 · CEC

Chemistry · 33d

Cleared May 05, 1982

TOTAL RADIOIMMUNOASSAY KIT

K821101 · CDX

Chemistry · 15d

Bioclinical Group - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Bioclinical Group

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