Medical Device Manufacturer · US , Mchenry , IL

Bio/Data Corp. - FDA 510(k) Cleared Devices

37 submissions · 37 cleared · Since 1977

Total

Cleared

Denied

Bio/Data Corp. has 37 FDA 510(k) cleared hematology devices. Based in Mchenry, US.

Historical record: 37 cleared submissions from 1977 to 2000.

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

Bio/Data 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 - Bio/Data Corp.

37 devices

1-12 of 37

Cleared Jul 12, 2000

MICROSAMPLE COAGULATION ANALYZER, MODEL MCA 310-C

K001891 · GKP

Hematology · 21d

Cleared Mar 24, 1995

MICROSAMPLE COAGULATION ANALYZER

K943153 · GKP

Hematology · 267d

Cleared Jun 23, 1989

PLATELET AGGREGATION PROFILER MODEL PAP-4C

K893650 · JPA

Hematology · 39d

Cleared Mar 28, 1988

KINETIC FIBRINOGEN ASSAY

K881150 · GIS

Hematology · 11d

Cleared Nov 20, 1987

PLATELET EXTRACT REAGENT

K873382 · GGW

Hematology · 88d

Cleared Mar 18, 1986

VON WILLEBRAND FAC. DEFIC. ABNORMAL CONTROL PLASMA

K860751 · JPK

Hematology · 18d

Cleared Mar 04, 1986

MICROSAMPLE COAGULATION ANALYSER, MODEL 110WP

K860342 · JPA

Hematology · 34d

Cleared Jan 07, 1986

MICROSAMPLE COAGULATION ANALYSER MODEL 110P

CEPHALINEX ACTIVATED PTT REAGENT

Looking for a specific device from Bio/Data Corp.? Search by device name or K-number.

Search all Bio/Data Corp. devices

Bio/Data Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Bio/Data Corp.

Filters