Last synced on 25 January 2026 at 3:41 am

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

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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