Product code BZT— Anesthesiology

ESOPHAGEAL STETHOSCOPE

Classification name
Stethoscope, Esophageal, With Electrical Conductors
Device class
Class 2
Regulation
21 CFR 868.1920
Advisory panel
Anesthesiology
Total cleared
46
First cleared
Most recent

Market context for product code BZT

FDA has cleared 46 devices under product code BZT between 1979 and 2025, filed by 34 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 BZT

Recent clearances under product code BZT

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