FDA Browser

Last synced on 18 April 2025 at 11:05 pm

subpart-f—therapeutic-devices/

OCU-FLEX-38 (POLYMACON)

Page Type: Cleared 510(K)
PDF: FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number: K941998
510(k) Type: Traditional
Applicant: OCU-EASE OPTICAL PRODUCTS, INC.
Country: United States
FDA Decision: Substantially Equivalent
Decision Date: 10/13/1994
Days to Decision: 171 days
Submission Type: Summary

FDA Browser

subpart-f—therapeutic-devices/

OCU-FLEX-38 (POLYMACON)

Page Type: Cleared 510(K)
PDF: FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number: K941998
510(k) Type: Traditional
Applicant: OCU-EASE OPTICAL PRODUCTS, INC.
Country: United States
FDA Decision: Substantially Equivalent
Decision Date: 10/13/1994
Days to Decision: 171 days
Submission Type: Summary