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NELLCOR OXIMAX N-600X PULSE OXIMETER, NELLCOR BEDSIDE RESPIRATORY PATIENT MONITORING SYSTEM, NELLCOR BEDSIDE SPO2 PATIEN

Page Type
Cleared 510(K)
510(k) Number
K123581
510(k) Type
Traditional
Applicant
COVIDIEN, FORMERLY NELLCOR PURITAN BENNETT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2013
Days to Decision
170 days
Submission Type
Summary

NELLCOR OXIMAX N-600X PULSE OXIMETER, NELLCOR BEDSIDE RESPIRATORY PATIENT MONITORING SYSTEM, NELLCOR BEDSIDE SPO2 PATIEN

Page Type
Cleared 510(K)
510(k) Number
K123581
510(k) Type
Traditional
Applicant
COVIDIEN, FORMERLY NELLCOR PURITAN BENNETT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2013
Days to Decision
170 days
Submission Type
Summary