Lansinoh Laboratories Saglik Gerecleri Tasarim San is one of 5703 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lansinoh Laboratories Saglik Gerecleri Tasarim San - FDA 510(k) Clear...
1
Total
1
Cleared
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Denied
Lansinoh Laboratories Saglik Gerecleri Tasarim San has 1 FDA 510(k) cleared medical devices. Based in Westminster, US.
Historical record: 1 cleared submissions from 2012 to 2012. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Lansinoh Laboratories Saglik Gerecleri Tasarim San Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lansinoh Laboratories Saglik Gerecleri Tasarim San
1 devices