Last synced on 25 January 2026 at 3:41 am

MICRO AMBULATORY ECG RECORDER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131572
510(k) Type
Traditional
Applicant
Dimetek Digital Medical Technologies, Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
7/22/2013
Days to Decision
52 days
Submission Type
Summary

MICRO AMBULATORY ECG RECORDER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131572
510(k) Type
Traditional
Applicant
Dimetek Digital Medical Technologies, Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
7/22/2013
Days to Decision
52 days
Submission Type
Summary