Product code FNP— General Hospital
MALE URINAL
- Classification name
- Urinal
- Device class
- Class 1
- Regulation
- 21 CFR 880.6730
- Advisory panel
- General Hospital
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code FNP
FDA has cleared device under product code FNP, all in 1977, filed by 1 applicant company. 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.
Top applicants under product code FNP
Recent clearances under product code FNP
Data sourced from openFDA. This site is unofficial and independent of the FDA.