DeviceClearance

Product code DQC— Cardiovascular

ACOUSTIC RECORDER

Classification name
Phonocardiograph
Device class
Class 1
Regulation
21 CFR 870.2390
Advisory panel
Cardiovascular
Total cleared
18
First cleared
Most recent

Market context for product code DQC

FDA has cleared 18 devices under product code DQC between 1976 and 1996, filed by 14 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 DQC

Recent clearances under product code DQC

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