SIMULSCOPE AUSCULTATION AND SIMULSCOPE BEDSIDE AUSCULTATION SYSTEM— 510(k) K961937

Name: FDA 510(k) clearance K961937
Creator: U.S. Food and Drug Administration
Published: 1996-12-09

Substantially Equivalent

Delphi Consulting Group

FDA 510(k) clearance K961937 for SIMULSCOPE AUSCULTATION AND SIMULSCOPE BEDSIDE AUSCULTATION SYSTEM, Substantially Equivalent on 1996-12-09. Applicant: Delphi Consulting Group. Device class: 2.

Clearance details

Applicant: Delphi Consulting Group
Product code: Code DQD
Device class: Class 2
Regulation: 21 CFR 870.1875
Advisory panel: Cardiovascular
Date received: 1996-05-20
Decision date: 1996-12-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, 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.