DeviceClearance

Product code KIN— Pathology

TEST, MONO., DIFFERENTIAL SLIDE

Classification name
Slide Stainer, Contact Type
Device class
Class 1
Regulation
21 CFR 864.3800
Advisory panel
Pathology
Total cleared
1
First cleared
Most recent

Market context for product code KIN

FDA has cleared 1 device under product code KIN, all in 1976, 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 KIN

Recent clearances under product code KIN

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