MIDMARK DIAGNOSTICS IQMARK VITAL SIGNS MONITOR


Device Classification Name

monitor,physiological,patient(without arrhythmia detection or alarms)

510(k) Number K072516
Device Name MIDMARK DIAGNOSTICS IQMARK VITAL SIGNS MONITOR
Applicant
MIDMARK DIAGNOSTICS GROUP
3300 fujita street
torrance, 
CA 
90505

Applicant Contact tony capparelli
Regulation Number 870.2300
Classification Product Code
MWI  
Date Received 09/07/2007
Decision Date 10/18/2007
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

summary

summary

Type Traditional
Reviewed by Third Party Yes

Combination Product

No