Medical Device Manufacturer · US , Logan , UT

Hyclone Laboratories, Inc. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 1987

Total

Cleared

Denied

Hyclone Laboratories, Inc. has 11 FDA 510(k) cleared pathology devices. Based in Logan, US.

Historical record: 11 cleared submissions from 1987 to 1988.

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

Hyclone Laboratories, 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 - Hyclone Laboratories, Inc.

11 devices

1-11 of 11

BOVINE CALF SERUM SUPPLEMENTED #A-2159

K880471 · KIS

Pathology · 61d

Cleared Apr 01, 1988

BOVINE CALF SERUM CATALOG #A-2119

DEFINED FETAL BOVINE SERUM #A-1111

K870463 · KIS

Pathology · 49d

Cleared Mar 24, 1987

CHARACTERIZED FETAL BOVINE SERUM #A-1115

K870464 · KIS

Pathology · 49d

Cleared Mar 24, 1987

6/40 FETAL BOVINE SERUM #A-1110

K870465 · KIS

Pathology · 49d

Cleared Mar 24, 1987

DEFINED CALF BOVINE SERUM #A-2111

K870466 · KIS

Pathology · 49d

Cleared Mar 24, 1987

DEFINED CALF BOVINE SERUM SUPPLEMENTED #A-2151

DEFINED EQUINE SERUM #A-3311

K870469 · KIS

Pathology · 49d

Hyclone Laboratories, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Hyclone Laboratories, Inc.

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