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SuperNO2VA Et Device

Page Type
Cleared 510(K)
510(k) Number
K173147
510(k) Type
Traditional
Applicant
Revolutionary Medical Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2018
Days to Decision
264 days
Submission Type
Summary

SuperNO2VA Et Device

Page Type
Cleared 510(K)
510(k) Number
K173147
510(k) Type
Traditional
Applicant
Revolutionary Medical Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2018
Days to Decision
264 days
Submission Type
Summary