Last synced on 23 February 2024 at 11:04 pm

REMI AI Discrete Detection Module

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231779
510(k) Type
Traditional
Applicant
Epitel, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/2024
Days to Decision
201 days
Submission Type
Summary

REMI AI Discrete Detection Module

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231779
510(k) Type
Traditional
Applicant
Epitel, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/2024
Days to Decision
201 days
Submission Type
Summary