Last synced on 18 April 2025 at 11:05 pm

DYNAPULSE 5000A MINI ABP BLOOD PRESSURE MONITORING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013358
510(k) Type
Special
Applicant
PULSE METRIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2001
Days to Decision
64 days
Submission Type
Statement

DYNAPULSE 5000A MINI ABP BLOOD PRESSURE MONITORING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013358
510(k) Type
Special
Applicant
PULSE METRIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2001
Days to Decision
64 days
Submission Type
Statement