CARDIOPHONICS INCORPORATED DPS 2000 PHONOCARDIOGRAPH— 510(k) K950537

Name: FDA 510(k) clearance K950537
Creator: U.S. Food and Drug Administration
Published: 1996-03-01

Substantially Equivalent

Cardiophonics, Inc.

FDA 510(k) clearance K950537 for CARDIOPHONICS INCORPORATED DPS 2000 PHONOCARDIOGRAPH, Substantially Equivalent on 1996-03-01. Applicant: Cardiophonics, Inc.. Device class: 1.

Clearance details

Applicant: Cardiophonics, Inc.
Product code: Code DQC
Device class: Class 1
Regulation: 21 CFR 870.2390
Advisory panel: Cardiovascular
Date received: 1995-02-07
Decision date: 1996-03-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Port Jefferson Station, NY, US

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