Product code KIO— Pathology
LINISTAIN SLS
- Classification name
- Slide Stainer, Immersion Type
- Device class
- Class 1
- Regulation
- 21 CFR 864.3800
- Advisory panel
- Pathology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code KIO
FDA has cleared device under product code KIO, all in 1989, 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 KIO
Recent clearances under product code KIO
Data sourced from openFDA. This site is unofficial and independent of the FDA.