Product code KCO— Ear, Nose, Throat
SYN-O-SCOPE NASAL INHALER
- Classification name
- Nasal Spray, Ent Delivery
- Device class
- Class 1
- Regulation
- 21 CFR 874.5220
- Advisory panel
- Ear, Nose, Throat
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code KCO
FDA has cleared device under product code KCO, 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 KCO
Recent clearances under product code KCO
Data sourced from openFDA. This site is unofficial and independent of the FDA.