Medical Device Manufacturer · US , Plano , TX

Hematronix, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1990

Total

Cleared

Denied

Hematronix, Inc. has 9 FDA 510(k) cleared medical devices. Based in Plano, US.

Historical record: 9 cleared submissions from 1990 to 2001. Primary specialty: Hematology.

Browse the FDA 510(k) cleared devices submitted by Hematronix, Inc. Filter by specialty or product code using the sidebar.

Hematronix, 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 - Hematronix, Inc.

9 devices

1-9 of 9

Cleared Aug 20, 2001

MCC URICHECK ASSAYED LIQUID URINE MULTICONSTITUENT CONTROL

CENTRIFIQ BLOOD CONTROL

Hematronix, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Hematronix, Inc.

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