Product code DSF— Cardiovascular

1,2,3 CHANNELL RECORDERS (AR150,AR250,-)

Classification name
Recorder, Paper Chart
Device class
Class 1
Regulation
21 CFR 870.2810
Advisory panel
Cardiovascular
Total cleared
87
First cleared
Most recent

Market context for product code DSF

FDA has cleared 87 devices under product code DSF between 1976 and 1991, filed by 55 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

last 15 years

Top applicants under product code DSF

Recent clearances under product code DSF

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