Slater Endoscopy, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Slater Endoscopy, LLC - FDA 510(k) Cleared Devices
Recent clearances: Ensizor Monopolar Endoscopic Scissors
3
Total
3
Cleared
0
Denied
Slater Endoscopy, LLC has 3 FDA 510(k) cleared medical devices. Based in Melbourne, US.
Historical record: 3 cleared submissions from 2014 to 2018. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Slater Endoscopy, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by C2c Development, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Slater Endoscopy, LLC
3 devices