FIW · Class II · 21 CFR 876.5820

FDA Product Code FIW: Alarm, Pillow Pressure

Leading manufacturers include Cordis Corp..

1
Total
1
Cleared
30d
Avg days
1978
Since

FDA 510(k) Cleared Alarm, Pillow Pressure Devices (Product Code FIW)

1 devices
1–1 of 1
Cleared Jan 26, 1978
BLOOD LINE COMP. NEG. PRESS. PILLOW
K772355
Cordis Corp.
Gastroenterology & Urology · 30d

About Product Code FIW - Regulatory Context