Last synced on 14 November 2025 at 11:06 pm

Mortara Surveyor Patient Monitor

Page Type
Cleared 510(K)
510(k) Number
K161517
510(k) Type
Traditional
Applicant
MORTARA INSTRUMENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/11/2017
Days to Decision
223 days
Submission Type
Summary

Mortara Surveyor Patient Monitor

Page Type
Cleared 510(K)
510(k) Number
K161517
510(k) Type
Traditional
Applicant
MORTARA INSTRUMENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/11/2017
Days to Decision
223 days
Submission Type
Summary