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DYNAPULSE 5200A PATHWAY BLOOD PRESSURE MONITORING SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013478
510(k) Type
Special
Applicant
Pulse Metric, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2002
Days to Decision
83 days
Submission Type
Statement

DYNAPULSE 5200A PATHWAY BLOOD PRESSURE MONITORING SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013478
510(k) Type
Special
Applicant
Pulse Metric, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2002
Days to Decision
83 days
Submission Type
Statement