Medical Device Manufacturer · US , Alameda , CA

Celera Diagnostics - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2007

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Celera Diagnostics Pathology ✕

1 devices

1-1 of 1

Cleared Sep 07, 2007

CYSTIC FIBROSIS GENOTYPING ASSAY, MODEL 6L20-01

Pathology · 416d