Medical Device Manufacturer · US , Mchenry , IL

Greene & Kellogg, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1980
4
Total
4
Cleared
0
Denied

Greene & Kellogg, Inc. has 4 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 4 cleared submissions from 1980 to 1983. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Greene & Kellogg, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Greene & Kellogg, Inc.

4 devices
1-4 of 4
Cleared Nov 29, 1983
BUNN MICRO OXYGEN CONCENTRATOR
K833495 · CAW
Anesthesiology · 53d
Cleared Feb 07, 1983
MODEL HI-FLO2 OXYGEN RICH AIR SUPPLY
K830046 · CAW
Anesthesiology · 28d
Cleared May 05, 1981
MODEL RXO2 OXYGEN RICH AIR SUPPLY
K811155 · CAW
Anesthesiology · 7d
Cleared Mar 25, 1980
MODEL 52 BUNN DRY AIR SUPPLY
K800534 · BTI
Anesthesiology · 18d
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