Product code IFT— Pathology
AD PERFECT
- Classification name
- Glutaraldehyde
- Device class
- Class 1
- Regulation
- 21 CFR 864.4010
- Advisory panel
- Pathology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code IFT
FDA has cleared device under product code IFT, all in 1995, 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 IFT
Recent clearances under product code IFT
Data sourced from openFDA. This site is unofficial and independent of the FDA.