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Hyper GP (tisilfocon A) Daily Wear Contact Lens

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182304
510(k) Type
Traditional
Applicant
CONTAMAC LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
11/23/2018
Days to Decision
91 days
Submission Type
Summary

Hyper GP (tisilfocon A) Daily Wear Contact Lens

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182304
510(k) Type
Traditional
Applicant
CONTAMAC LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
11/23/2018
Days to Decision
91 days
Submission Type
Summary