WASHINGTON CARDIAC MONITOR— 510(k) K903710

Name: FDA 510(k) clearance K903710
Creator: U.S. Food and Drug Administration
Published: 1990-11-09

Substantially Equivalent

Washington Biolab, Inc.

FDA 510(k) clearance K903710 for WASHINGTON CARDIAC MONITOR, Substantially Equivalent on 1990-11-09. Applicant: Washington Biolab, Inc.. Device class: 2.

Clearance details

Applicant: Washington Biolab, Inc.
Product code: Code DXK
Device class: Class 2
Regulation: 21 CFR 870.2330
Advisory panel: Cardiovascular
Date received: 1990-08-14
Decision date: 1990-11-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ames, IA, US

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