Medical Device Manufacturer · US , Lexington , MA

W.R. Grace & Co.-Conn. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1986

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - W.R. Grace & Co.-Conn. Gastroenterology & Urology ✕

1 devices

1-1 of 1

Cleared Dec 09, 1987

MODIFIED HOLLOW FIBERS USED IN DIAFILTER HEMOFIL.

Gastroenterology & Urology · 77d