FDA Browser

Last synced on 6 June 2025 at 11:06 pm

subpart-f—therapeutic-devices/

ACUVUE OASYS (senofilcon A) with Photochromic Additive

Page Type: Cleared 510(K)
PDF: FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number: K180299
510(k) Type: Traditional
Applicant: Johnson & Johnson Vision Care, Inc.
Country: United States
FDA Decision: Substantially Equivalent
Decision Date: 4/10/2018
Days to Decision: 67 days
Submission Type: Summary

FDA Browser

subpart-f—therapeutic-devices/

ACUVUE OASYS (senofilcon A) with Photochromic Additive

Page Type: Cleared 510(K)
PDF: FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number: K180299
510(k) Type: Traditional
Applicant: Johnson & Johnson Vision Care, Inc.
Country: United States
FDA Decision: Substantially Equivalent
Decision Date: 4/10/2018
Days to Decision: 67 days
Submission Type: Summary