Cleared Traditional

K841574 - QUAZAR ESOPHAGEAL STETHOSCOPE
(FDA 510(k) Clearance)

Aug 1984
Decision
120d
Days
Class 1
Risk

K841574 is an FDA 510(k) clearance for the QUAZAR ESOPHAGEAL STETHOSCOPE. This device is classified as a Stethoscope, Esophageal (Class I - General Controls, product code BZW).

Submitted by Axiom Medical, Inc. (Mchenry, US). The FDA issued a Cleared decision on August 15, 1984, 120 days after receiving the submission on April 17, 1984.

This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.1910.

Submission Details

510(k) Number K841574 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 17, 1984
Decision Date August 15, 1984
Days to Decision 120 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary

Device Classification

Product Code BZW — Stethoscope, Esophageal
Device Class Class I - General Controls
CFR Regulation 21 CFR 868.1910