DeviceClearance

Product code KIT— Hematology

DULBECCO'S MODIFIED EAGLE'S MEDIUM (DME)

Classification name
Media And Components, Synthetic Cell And Tissue Culture
Device class
Class 1
Regulation
21 CFR 864.2220
Advisory panel
Hematology
Total cleared
367
First cleared
Most recent

Market context for product code KIT

FDA has cleared 367 devices under product code KIT between 1977 and 1989, filed by 33 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 KIT

Recent clearances under product code KIT

1–100 of 367

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