Product code DQD— Cardiovascular

STETHOSCOPE

Classification name
Stethoscope, Electronic
Device class
Class 2
Regulation
21 CFR 870.1875
Advisory panel
Cardiovascular
Total cleared
156
First cleared
Most recent

Market context for product code DQD

FDA has cleared 156 devices under product code DQD between 1977 and 2026, filed by 102 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 DQD

Recent clearances under product code DQD

1–100 of 156

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