Medical Device Manufacturer · US , Palatine , IL

Sellstrom Mfg. Co.

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

Sellstrom Mfg. Co. — FDA 510(k) Submissions

Sellstrom Mfg. Co. has submitted 2 FDA 510(k) premarket notifications since 1993, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Shield, Eye, Ophthalmic (including Sunlamp Protective Eyewear And Post-mydriatic Eyewear) . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
Filters
All2 Ophthalmic 2