Semperit Technische Produkte Gesellchaft M.B.H. is one of 30 FDA 510(k) medical device manufacturers from Austria in the dataset, ranked by real submission volume.
Semperit Technische Produkte Gesellchaft M.B.H. - FDA 510(k) Cleared ...
Recent clearances: Sterile Powder-Free Synthetic Rubber Surgeon’s Glove with Low Dermatitis Potential
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Semperit Technische Produkte Gesellchaft M.B.H. has 1 FDA 510(k) cleared medical devices. Based in Wimpassing, AT.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Semperit Technische Produkte Gesellchaft M.B.H. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mansour Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Semperit Technische Produkte Gesellchaft M.B.H.
1 devices