Last synced on 14 November 2025 at 11:06 pm

INVOS PM7100 Patient Monitor, INVOS Adult rSO2 Sensor

Page Type
Cleared 510(K)
510(k) Number
K182868
510(k) Type
Traditional
Applicant
Covidien llc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/2019
Days to Decision
88 days
Submission Type
Summary

INVOS PM7100 Patient Monitor, INVOS Adult rSO2 Sensor

Page Type
Cleared 510(K)
510(k) Number
K182868
510(k) Type
Traditional
Applicant
Covidien llc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/2019
Days to Decision
88 days
Submission Type
Summary