Medical Device Manufacturer · US , Palatine , IL

Sellstrom Mfg. Co. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1993
2
Total
2
Cleared
0
Denied

Sellstrom Mfg. Co. has 2 FDA 510(k) cleared medical devices. Based in Palatine, US.

Historical record: 2 cleared submissions from 1993 to 1994. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Sellstrom Mfg. Co. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Sellstrom Mfg. Co.

2 devices
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