DYNAMIC SPECTRAL PHONOCARDIOGRAPH— 510(k) K902185

Name: FDA 510(k) clearance K902185
Creator: U.S. Food and Drug Administration
Published: 1991-03-25

Substantially Equivalent

Reeves Scientific, Inc.

FDA 510(k) clearance K902185 for DYNAMIC SPECTRAL PHONOCARDIOGRAPH, Substantially Equivalent on 1991-03-25. Applicant: Reeves Scientific, Inc.. Device class: 1.

Clearance details

Applicant: Reeves Scientific, Inc.
Product code: Code DQC
Device class: Class 1
Regulation: 21 CFR 870.2390
Advisory panel: Cardiovascular
Date received: 1990-05-14
Decision date: 1991-03-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New Haven, CT, US

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