Last synced on 2 June 2023 at 11:04 pm

NOVAVISION, MODEL 2.0

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023623
510(k) Type
Traditional
Applicant
NOVAVISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/2003
Days to Decision
175 days
Submission Type
Summary

NOVAVISION, MODEL 2.0

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023623
510(k) Type
Traditional
Applicant
NOVAVISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/2003
Days to Decision
175 days
Submission Type
Summary