ANGIONEW-IV


Device Classification Name

device, counter-pulsating, external

510(k) Number K023701
Device Name ANGIONEW-IV
Original Applicant
LIVING DATA TECHNOLOGIES CORPORATION
55 northern blvd. suite 200
great neck, 
NY 
11021

Original Contact susan d goldstein-falk
Regulation Number 870.5225
Classification Product Code
DRN  
Date Received 11/04/2002
Decision Date 01/30/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No