Medical Device Manufacturer · US , Mchenry , IL

The Kendall Company Div. of Tyco Healthcare Group - FDA 510(k) Cleare...

4 submissions · 4 cleared · Since 1983
4
Total
4
Cleared
0
Denied

The Kendall Company Div. of Tyco Healthcare Group has 4 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 4 cleared submissions from 1983 to 2003.

Browse the FDA 510(k) cleared devices submitted by The Kendall Company Div. of Tyco Healthcare Group Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - The Kendall Company Div. of Tyco Healthcare Group

4 devices
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