DeviceClearance

Product code KNG— Obstetrics/Gynecology

Fetal Doppler

Classification name
Monitor, Ultrasonic, Fetal
Device class
Class 2
Regulation
21 CFR 884.2660
Advisory panel
Obstetrics/Gynecology
Total cleared
60
First cleared
Most recent

Market context for product code KNG

FDA has cleared 60 devices under product code KNG between 1976 and 2026, filed by 43 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

last 15 years

Top applicants under product code KNG

Recent clearances under product code KNG

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