Last synced on 2 May 2025 at 11:05 pm

DMS 300-2W HOLTER ECG RECORDER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133014
510(k) Type
Special
Applicant
DIAGNOSTIC MONITORING SOFTWARE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/2014
Days to Decision
236 days
Submission Type
Summary

DMS 300-2W HOLTER ECG RECORDER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K133014
510(k) Type
Special
Applicant
DIAGNOSTIC MONITORING SOFTWARE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/2014
Days to Decision
236 days
Submission Type
Summary