Medical Device Manufacturer · US , Mchenry , IL

Hankscraft Div. of Gerber Products Co. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1979

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Hankscraft Div. of Gerber Products Co. Anesthesiology ✕

1 devices

1-1 of 1

Cleared Jun 11, 1979

ULTRASONIC HUMIDIFIER

Anesthesiology · 20d