Last synced on 18 July 2025 at 11:06 pm

NUVANT CARDIAC EVENT MONITORING SYSTEM; NUVANT MOBILE CARDIAC TELEMETRY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090696
510(k) Type
Special
Applicant
CORVENTIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/2009
Days to Decision
95 days
Submission Type
Summary

NUVANT CARDIAC EVENT MONITORING SYSTEM; NUVANT MOBILE CARDIAC TELEMETRY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090696
510(k) Type
Special
Applicant
CORVENTIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/2009
Days to Decision
95 days
Submission Type
Summary