Last synced on 18 April 2025 at 11:05 pm

ULTRAVUE/P, ULTRALVUE/C (HIOXIFILCON B)) SOFT (MULTIFOCAL) DAILY WEAR CONTACT LENS (CLEAR & YINTED, LATHE-CUT FROM LENS)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K974599
510(k) Type
Traditional
Applicant
OPTI-CENTRE LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/1998
Days to Decision
83 days
Submission Type
Summary

ULTRAVUE/P, ULTRALVUE/C (HIOXIFILCON B)) SOFT (MULTIFOCAL) DAILY WEAR CONTACT LENS (CLEAR & YINTED, LATHE-CUT FROM LENS)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K974599
510(k) Type
Traditional
Applicant
OPTI-CENTRE LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/1998
Days to Decision
83 days
Submission Type
Summary