Stihler Electronic, C/O Worldwide Regul. Services is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stihler Electronic, C/O Worldwide Regul. Services - FDA 510(k) Cleare...
1
Total
1
Cleared
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Denied
Stihler Electronic, C/O Worldwide Regul. Services has 1 FDA 510(k) cleared medical devices. Based in Farmingville, US.
Historical record: 1 cleared submissions from 1988 to 1988. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Stihler Electronic, C/O Worldwide Regul. Services Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Stihler Electronic, C/O Worldwide Regul. Services
1 devices