HL 200 ELECTRONIC STETHOSCOPE— 510(k) K050169

Name: FDA 510(k) clearance K050169
Creator: U.S. Food and Drug Administration
Published: 2005-04-05

Substantially Equivalent

Health & Life Co., Ltd.

FDA 510(k) clearance K050169 for HL 200 ELECTRONIC STETHOSCOPE, Substantially Equivalent on 2005-04-05. Applicant: Health & Life Co., Ltd.. Device class: 2.

Clearance details

Applicant: Health & Life Co., Ltd.
Product code: Code DQD
Device class: Class 2
Regulation: 21 CFR 870.1875
Advisory panel: Cardiovascular
Date received: 2005-01-26
Decision date: 2005-04-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Flagstaff, AZ, US

Download summary PDF View on FDA.gov ↗

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