Last synced on 30 September 2022 at 11:05 pm

REMI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203827
510(k) Type
Traditional
Applicant
Epitel, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/2021
Days to Decision
90 days
Submission Type
Summary

REMI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203827
510(k) Type
Traditional
Applicant
Epitel, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/2021
Days to Decision
90 days
Submission Type
Summary