NUVANT, MOBILE CARDIAC TELEMETRY


Device Classification Name

monitor, physiological, patient(with arrhythmia detection or alarms)

510(k) Number K111917
Device Name NUVANT, MOBILE CARDIAC TELEMETRY
Applicant
CORVENTIS, INC.
1410 energy park drive,
suite 1
st. paul, 
MN 
55108

Applicant Contact michele chin-purcell
Correspondent
CORVENTIS, INC.
1410 energy park drive,
suite 1
st. paul, 
MN 
55108

Correspodent Contact michele chin-purcell
Regulation Number 870.1025
Classification Product Code
MHX  
Date Received 07/06/2011
Decision Date 08/24/2011
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

summary

summary

Type Abbreviated
Reviewed by Third Party No

Combination Product

No