VERTEX SYSTEM


information about

Device Classification Name

electrocardiograph

510(k) Number K002822
Device Name VERTEX SYSTEM
Original Applicant
MEDICAL POSITIONING, INC.
21911 erie ln.
lake forest, 
CA 
92630

Original Contact carol patterson
Regulation Number 870.2340
Classification Product Code
DPS  
Date Received 09/11/2000
Decision Date 01/31/2001
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

Type Traditional
Reviewed by Third Party No

Combination Product

No