MOBILE EXTERNAL COUNTER PULSATION SYSTEM ANGIONEW-V— 510(k) K033657

Name: FDA 510(k) clearance K033657
Creator: U.S. Food and Drug Administration
Published: 2003-12-19

Substantially Equivalent

Living Data Technologies Corporation

FDA 510(k) clearance K033657 for MOBILE EXTERNAL COUNTER PULSATION SYSTEM ANGIONEW-V, Substantially Equivalent on 2003-12-19. 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: 2003-11-21
Decision date: 2003-12-19
Decision: Substantially Equivalent
Clearance type: Special
Location: Great Neck, NY, US

Download summary PDF View on FDA.gov ↗

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