Medical Device Manufacturer · US , Fort Myers , FL

Intertech Resources, Inc. - FDA 510(k) Cleared Devices

29 submissions · 27 cleared · Since 1987
29
Total
27
Cleared
0
Denied

Intertech Resources, Inc. has 27 FDA 510(k) cleared anesthesiology devices. Based in Fort Myers, US.

Historical record: 27 cleared submissions from 1987 to 1996.

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 - Intertech Resources, Inc.
29 devices
1-12 of 29
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