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CENTURION 2000 CENTRAL STATION ARRHYTHMIA PATIENT MONITORING SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002604
510(k) Type
Traditional
Applicant
Invivo Research, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/2002
Days to Decision
534 days
Submission Type
Summary

CENTURION 2000 CENTRAL STATION ARRHYTHMIA PATIENT MONITORING SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002604
510(k) Type
Traditional
Applicant
Invivo Research, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/2002
Days to Decision
534 days
Submission Type
Summary