Last synced on 20 December 2024 at 11:05 pm

OptikView GUP2103CMI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191705
510(k) Type
Traditional
Applicant
The Linden Group Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/2020
Days to Decision
264 days
Submission Type
Summary

OptikView GUP2103CMI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191705
510(k) Type
Traditional
Applicant
The Linden Group Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/2020
Days to Decision
264 days
Submission Type
Summary