Medical Device Manufacturer · US , Mchenry , IL

Gould, Inc. - FDA 510(k) Cleared Devices

31 submissions · 31 cleared · Since 1976

31

Total

31

Cleared

0

Denied

FDA 510(k) Regulatory Record - Gould, Inc. Anesthesiology ✕

2 devices

1-2 of 2

Cleared Jan 14, 1986

MODEL 2120 SPIROSCREEN

Anesthesiology · 75d

Cleared Oct 24, 1984

MODEL IM1074 END-TIDAL CO2 MODULE

Anesthesiology · 13d