ANGIONEW-IV— 510(k) K023701

Name: FDA 510(k) clearance K023701
Creator: U.S. Food and Drug Administration
Published: 2003-01-30

Substantially Equivalent

Living Data Technologies Corporation

FDA 510(k) clearance K023701 for ANGIONEW-IV, Substantially Equivalent on 2003-01-30. Applicant: Living Data Technologies Corporation. Device class: 2.

Clearance details

Applicant: Living Data Technologies Corporation
Product code: Code DRN
Device class: Class 2
Regulation: 21 CFR 870.5225
Advisory panel: Cardiovascular
Date received: 2002-11-04
Decision date: 2003-01-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck, NY, US

Download summary PDF View on FDA.gov ↗

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