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subpart-f—therapeutic-devices/

GELFLEX TRITON HW SOFT BIFOCAL CONTACT LENS AND THE GELFLEX TRITON SOFT BIFOCAL CONTACT LENS

Page Type: Cleared 510(K)
PDF: FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number: K011072
510(k) Type: Traditional
Applicant: GELFLEX
Country: Australia
FDA Decision: Substantially Equivalent
Decision Date: 8/24/2001
Days to Decision: 137 days
Submission Type: Summary

FDA Browser

subpart-f—therapeutic-devices/

GELFLEX TRITON HW SOFT BIFOCAL CONTACT LENS AND THE GELFLEX TRITON SOFT BIFOCAL CONTACT LENS

Page Type: Cleared 510(K)
PDF: FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number: K011072
510(k) Type: Traditional
Applicant: GELFLEX
Country: Australia
FDA Decision: Substantially Equivalent
Decision Date: 8/24/2001
Days to Decision: 137 days
Submission Type: Summary