Medical Device Manufacturer · US , Irvine , CA

I-Flow Corp. - FDA 510(k) Cleared Devices

41 submissions · 41 cleared · Since 1988
41
Total
41
Cleared
0
Denied

I-Flow Corp. has 41 FDA 510(k) cleared general hospital devices. Based in Irvine, US.

Historical record: 41 cleared submissions from 1988 to 2007.

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

FDA 510(k) Regulatory Record - I-Flow Corp.
41 devices
1-12 of 41

Looking for a specific device from I-Flow Corp.? Search by device name or K-number.

Search all I-Flow Corp. devices
Filters