Product code KCQ— Dental
L.T.C. REPLACEMENT GASTROSTOMY TUBE
- Classification name
- Tube Impression And Matrix
- Device class
- Class 1
- Regulation
- 21 CFR 872.6570
- Advisory panel
- Dental
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code KCQ
FDA has cleared device under product code KCQ, all in 1990, 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 KCQ
Recent clearances under product code KCQ
Data sourced from openFDA. This site is unofficial and independent of the FDA.