Product code KZB— Microbiology
TWIN-FUSOR/UNI-FUSOR BLOOD & FLUID INFUSION CUFF
- Classification name
- Automated Colony Counter
- Device class
- Class 1
- Regulation
- 21 CFR 866.2170
- Advisory panel
- Microbiology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code KZB
FDA has cleared device under product code KZB, 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 KZB
Recent clearances under product code KZB
Data sourced from openFDA. This site is unofficial and independent of the FDA.