Last synced on 25 January 2026 at 3:41 am

SENTORR ARTERIAL PRESSURE SENSOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880830
510(k) Type
Traditional
Applicant
OHMEDA MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1988
Days to Decision
164 days

SENTORR ARTERIAL PRESSURE SENSOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880830
510(k) Type
Traditional
Applicant
OHMEDA MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1988
Days to Decision
164 days