Last synced on 23 September 2022 at 11:05 pm

KERATOREF L60

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K922253
510(k) Type
Traditional
Applicant
LUNEAU OPHTALMOLOGIE SA
Country
France
FDA Decision
Substantially Equivalent
Decision Date
6/19/1992
Days to Decision
49 days
Submission Type
Statement

KERATOREF L60

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K922253
510(k) Type
Traditional
Applicant
LUNEAU OPHTALMOLOGIE SA
Country
France
FDA Decision
Substantially Equivalent
Decision Date
6/19/1992
Days to Decision
49 days
Submission Type
Statement