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subpart-f—therapeutic-devices/

LL BI-FOCAL, 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: K971647
510(k) Type: Traditional
Applicant: LOMBART LENSES, LTD.
Country: United States
FDA Decision: Substantially Equivalent
Decision Date: 7/15/1997
Days to Decision: 71 days
Submission Type: Statement

FDA Browser

subpart-f—therapeutic-devices/

LL BI-FOCAL, 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: K971647
510(k) Type: Traditional
Applicant: LOMBART LENSES, LTD.
Country: United States
FDA Decision: Substantially Equivalent
Decision Date: 7/15/1997
Days to Decision: 71 days
Submission Type: Statement