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RMU-2000 Automated Chest Compression System

Page Type
Cleared 510(K)
510(k) Number
K211289
510(k) Type
Traditional
Applicant
Defibtech, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/2021
Days to Decision
195 days
Submission Type
Summary

RMU-2000 Automated Chest Compression System

Page Type
Cleared 510(K)
510(k) Number
K211289
510(k) Type
Traditional
Applicant
Defibtech, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/2021
Days to Decision
195 days
Submission Type
Summary