Last synced on 30 November 2024 at 11:09 am

SuperNO2VA Et Device

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