Last synced on 2 May 2025 at 11:05 pm

DIGITAL AMBULATORY ECG (HOLTER) RECORDER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031074
510(k) Type
Traditional
Applicant
DATRIX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2003
Days to Decision
194 days
Submission Type
Summary

DIGITAL AMBULATORY ECG (HOLTER) RECORDER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031074
510(k) Type
Traditional
Applicant
DATRIX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2003
Days to Decision
194 days
Submission Type
Summary