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

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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