Medical Device Manufacturer · US , Mchenry , IL

American Pacemaker Corp. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1977
14
Total
14
Cleared
0
Denied

American Pacemaker Corp. has 14 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.

Historical record: 14 cleared submissions from 1977 to 1982.

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

FDA 510(k) Regulatory Record - American Pacemaker Corp.
14 devices
1-14 of 14
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