Product code JKP— Clinical Chemistry
API TURBICITY STANDARD
- Classification name
- Chromium-51, Blood Volume
- Device class
- Class 1
- Regulation
- 21 CFR 862.1130
- Advisory panel
- Clinical Chemistry
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code JKP
FDA has cleared device under product code JKP, all in 1981, 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 JKP
Recent clearances under product code JKP
Data sourced from openFDA. This site is unofficial and independent of the FDA.