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SuperNO2VA Device

Page Type
Cleared 510(K)
510(k) Number
K163277
510(k) Type
Traditional
Applicant
Revolutionary Medical Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/13/2017
Days to Decision
326 days
Submission Type
Summary

SuperNO2VA Device

Page Type
Cleared 510(K)
510(k) Number
K163277
510(k) Type
Traditional
Applicant
Revolutionary Medical Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/13/2017
Days to Decision
326 days
Submission Type
Summary