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BEDSIDE RESPIRATORY PATIENT MONITORING SYSTEM, BEDSIDE RESPIRATORY PATIENT MONITORING SYSTEM WITH RESPIRATION RATE SOFTW

Page Type
Cleared 510(K)
510(k) Number
K130320
510(k) Type
Traditional
Applicant
COVIDIEN
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/2014
Days to Decision
361 days
Submission Type
Summary

BEDSIDE RESPIRATORY PATIENT MONITORING SYSTEM, BEDSIDE RESPIRATORY PATIENT MONITORING SYSTEM WITH RESPIRATION RATE SOFTW

Page Type
Cleared 510(K)
510(k) Number
K130320
510(k) Type
Traditional
Applicant
COVIDIEN
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/2014
Days to Decision
361 days
Submission Type
Summary