Product code KET— Pathology
CORNING DISPOSAL STERILE FILTER SYSTEM-NYLON
- Classification name
- Filters, Cell Collection, Tissue Processing
- Device class
- Class 1
- Regulation
- 21 CFR 864.3010
- Advisory panel
- Pathology
- Total cleared
- 5
- First cleared
- Most recent
Market context for product code KET
FDA has cleared devices under product code KET between 1980 and 1988, filed by 3 applicant companies. 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.
Clearances per year
- 1988
- 1987
- 1985
- 1984
- 1980
Top applicants under product code KET
Recent clearances under product code KET
Data sourced from openFDA. This site is unofficial and independent of the FDA.