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PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K120631
510(k) Type
Traditional
Applicant
ADVANCED INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/2012
Days to Decision
85 days
Submission Type
Summary

PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K120631
510(k) Type
Traditional
Applicant
ADVANCED INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/25/2012
Days to Decision
85 days
Submission Type
Summary