CENTURY SERIES HOLTER SCANNER SYSTEM, MODELS C3000, C2000 AND C1000— 510(k) K024323

Name: FDA 510(k) clearance K024323
Creator: U.S. Food and Drug Administration
Published: 2003-06-30

Substantially Equivalent

Biomedical Systems Corp.

FDA 510(k) clearance K024323 for CENTURY SERIES HOLTER SCANNER SYSTEM, MODELS C3000, C2000 AND C1000, Substantially Equivalent on 2003-06-30. Applicant: Biomedical Systems Corp.. Device class: 2.

Clearance details

Applicant: Biomedical Systems Corp.
Product code: Code MLO
Device class: Class 2
Regulation: 21 CFR 870.2800
Advisory panel: Cardiovascular
Date received: 2002-12-26
Decision date: 2003-06-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Louis, MO, US

Download summary PDF View on FDA.gov ↗

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