Medical Device Manufacturer · US , Mchenry , IL

The John Bunn Co. - FDA 510(k) Cleared Devices

20 submissions · 20 cleared · Since 1976
20
Total
20
Cleared
0
Denied

The John Bunn Co. has 20 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.

Historical record: 20 cleared submissions from 1976 to 1990.

Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - The John Bunn Co.
20 devices
1-12 of 20
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