Product code FOA— General Hospital
ECA
- Classification name
- Board, Cardiopulmonary
- Device class
- Class 1
- Regulation
- 21 CFR 880.6080
- Advisory panel
- General Hospital
- Total cleared
- 3
- First cleared
- Most recent
Market context for product code FOA
FDA has cleared devices under product code FOA between 1981 and 2022, filed by 3 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 2022
- 2020
- 1981
Top applicants under product code FOA
Recent clearances under product code FOA
Data sourced from openFDA. This site is unofficial and independent of the FDA.