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TRUEPULSE DISPOSABLE INVASIVE BLOOD PRESSURE MONITORING KIT

Page Type
Cleared 510(K)
510(k) Number
K062342
510(k) Type
Traditional
Applicant
Sentra Medical Devices, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/2006
Days to Decision
45 days
Submission Type
Summary

TRUEPULSE DISPOSABLE INVASIVE BLOOD PRESSURE MONITORING KIT

Page Type
Cleared 510(K)
510(k) Number
K062342
510(k) Type
Traditional
Applicant
Sentra Medical Devices, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/2006
Days to Decision
45 days
Submission Type
Summary