CPRMETER CPR FEEDBACK DEVICE


Device Classification Name

aid, cardiopulmonary resuscitation

510(k) Number K122050
Device Name CPRMETER CPR FEEDBACK DEVICE
Applicant
LAERDAL MEDICAL A/S
1 geddes way
west lafayette, 
IN 
47906

Applicant Contact dan dillion
Correspondent
LAERDAL MEDICAL A/S
1 geddes way
west lafayette, 
IN 
47906

Correspodent Contact dan dillion
Regulation Number 870.5200
Classification Product Code
LIX  
Date Received 07/12/2012
Decision Date 10/22/2012
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No