Product code JTB— Microbiology
HI VOLUME PUMPING CHAMBER
- Classification name
- Device, Media Dispensing/Stacking
- Device class
- Class 1
- Regulation
- 21 CFR 866.2440
- Advisory panel
- Microbiology
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code JTB
FDA has cleared devices under product code JTB between 1979 and 1980, filed by 2 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
- 1980
- 1979
Top applicants under product code JTB
Recent clearances under product code JTB
Data sourced from openFDA. This site is unofficial and independent of the FDA.