Medical Device Manufacturer · US , Washington , DC

Tosoh Corp. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 1990

Recent clearances: AIA-PACK CA 19-9, ST AIA-PACK CA 19-9, AIA-1200DX - AUTOMATED ENZYME IMMUNOASSAY SYSTEM

View 11 510(k) Devices ↓ Official Website

11

Total

11

Cleared

0

Denied

FDA 510(k) Regulatory Record - Tosoh Corp. Hematology ✕

1 devices

1-1 of 1

Cleared Jul 21, 1992

AIA-1200DX - AUTOMATED ENZYME IMMUNOASSAY SYSTEM

Hematology · 28d