Certa Dose, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Certa Dose, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Certa Dose Pediatric Midazolam 5mg/mL IM Syringe
2
Total
2
Cleared
0
Denied
Certa Dose, Inc. has 2 FDA 510(k) cleared medical devices. Based in Dever, US.
Historical record: 2 cleared submissions from 2017 to 2018. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Certa Dose, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Epstein Becker & Green, P.C. as regulatory consultant.
FDA 510(k) Regulatory Record - Certa Dose, Inc.
2 devices