Medical Device Manufacturer · US , Riverside , CA

Bio Clinic Co. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1988

Total

Cleared

Denied

Bio Clinic Co. has 14 FDA 510(k) cleared medical devices. Based in Riverside, US.

Historical record: 14 cleared submissions from 1988 to 1993. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by Bio Clinic Co. Filter by specialty or product code using the sidebar.

Bio Clinic Co. 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 - Bio Clinic Co.

14 devices

1-12 of 14

Cleared Aug 06, 1993

AMERICAN POWER CONVERSIONS, BACK-UPS 600

K930791 · FMF

General Hospital · 171d

Cleared Jul 21, 1993

PRISM

K932480 · IOQ

Physical Medicine · 58d

Cleared Jun 24, 1993

ORTHODERM CONSUMMATE AIR THERAPY BED W/SCALE

K926189 · IOQ

Physical Medicine · 198d

ORTHODERM CONVERTIBLE II

K922140 · IOQ

Physical Medicine · 21d

Cleared May 07, 1992

NOW PREGNANCY TEST KIT

K921211 · JHI

Chemistry · 56d

Cleared May 07, 1992

MIRCO ELISA HPL TEST KIT

K921212 · JHI

Chemistry · 56d

Cleared Apr 08, 1992

ELISA TUBE LH TEST KIT

K920920 · CEP

Chemistry · 40d

Cleared Apr 08, 1992

ELISA TUBE PROLACTIN TEST KIT

K920921 · CFT

Chemistry · 40d

Cleared Apr 07, 1992

TMB CHROMOGEN/SUBSTRATE REAGENT SET

K920918 · JHI

Chemistry · 39d

Cleared Mar 26, 1992

ELISA TUBE FSH TEST KIT ENZYME LINKED IMMUN. ASSAY

K920917 · CGJ

Chemistry · 27d

Cleared Nov 27, 1990

BIO MEDX AIR FLOTATION SYSTEM

K905156 · IOQ

Physical Medicine · 12d

Bio Clinic Co. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Bio Clinic Co.

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