Product code IDW— Pathology
HISTO-CENTER II
- Classification name
- Dispensers, Paraffin
- Device class
- Class 1
- Regulation
- 21 CFR 864.3010
- Advisory panel
- Pathology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code IDW
FDA has cleared device under product code IDW, all in 1979, 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 IDW
Recent clearances under product code IDW
Data sourced from openFDA. This site is unofficial and independent of the FDA.