Medical Device Manufacturer · US , Kansas City , MO

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

3 submissions · 3 cleared · Since 1989

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Primus, Inc. Hematology ✕

2 devices

1-2 of 2

Cleared May 22, 2000

NYCOCARD HBA1C GLYCOSYLATED HEMOGLOBIN ASSAY

Hematology · 245d

Cleared Jun 16, 1989

PRIMUS MODEL CLC 330

Hematology · 101d