Nevap, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nevap, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NeVap Aspire Subglottic Suction Endotracheal Tube (ASSET) with Preloaded Stylet
1
Total
1
Cleared
0
Denied
Nevap, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Jose, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Nevap, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mae Consulting Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Nevap, Inc.
1 devices