DeviceClearance

Product code JSP— Microbiology

LYFO(TM) DIFFERENTIAL DISK

Classification name
Kit, Anaerobic Identification
Device class
Class 1
Regulation
21 CFR 866.2660
Advisory panel
Microbiology
Total cleared
18
First cleared
Most recent

Market context for product code JSP

FDA has cleared 18 devices under product code JSP between 1977 and 1995, filed by 12 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

Top applicants under product code JSP

Recent clearances under product code JSP

Data sourced from openFDA. This site is unofficial and independent of the FDA.