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SURVEYOR S4 MOBILE MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141020
510(k) Type
Traditional
Applicant
MORTARA INSTRUMENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/2014
Days to Decision
226 days
Submission Type
Summary

SURVEYOR S4 MOBILE MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141020
510(k) Type
Traditional
Applicant
MORTARA INSTRUMENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/2014
Days to Decision
226 days
Submission Type
Summary