MCPULSE


Device Classification Name

plethysmograph, photoelectric, pneumatic or hydraulic

510(k) Number K023238
Device Name MCPULSE
Original Applicant
MERIDIAN CO., LTD.
po box 7007
deerfield, 
IL 
60015

Original Contact daniel kamm
Regulation Number 870.2780
Classification Product Code
JOM  
Date Received 09/27/2002
Decision Date 02/19/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No