Medical Device Manufacturer · US , Mundelein , IL

Sitco, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1995
4
Total
4
Cleared
0
Denied

Sitco, Inc. has 4 FDA 510(k) cleared medical devices. Based in Mundelein, US.

Historical record: 4 cleared submissions from 1995 to 1999. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Sitco, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Sitco, Inc.
4 devices
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