Last synced on 25 January 2026 at 3:41 am

QRS CARD S-T SEGMENT ANALYSIS PATIENT MONITORING SYSTEM MODEL: QRS CARD USB

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100813
510(k) Type
Special
Applicant
Pulse Biomedical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2010
Days to Decision
122 days
Submission Type
Summary

QRS CARD S-T SEGMENT ANALYSIS PATIENT MONITORING SYSTEM MODEL: QRS CARD USB

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100813
510(k) Type
Special
Applicant
Pulse Biomedical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2010
Days to Decision
122 days
Submission Type
Summary