MIDMARK IQECG


Device Classification Name

electrocardiograph

510(k) Number K103640
Device Name MIDMARK IQECG
Applicant
BRENTWOOD MEDICAL TECHNOLOGY CORP.
3722 ave. sausalito
irvine, 
CA 
92606

Applicant Contact greg holland
Correspondent
BRENTWOOD MEDICAL TECHNOLOGY CORP.
3722 ave. sausalito
irvine, 
CA 
92606

Correspodent Contact greg holland
Regulation Number 870.2340
Classification Product Code
DPS  
Date Received 12/13/2010
Decision Date 03/22/2011
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No