Last synced on 30 September 2022 at 11:05 pm

EYECHEK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964290
510(k) Type
Traditional
Applicant
REICHERT OPHTHALMIC INSTRUMENTS, DIV. LEICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/1997
Days to Decision
73 days
Submission Type
Statement

EYECHEK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964290
510(k) Type
Traditional
Applicant
REICHERT OPHTHALMIC INSTRUMENTS, DIV. LEICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/1997
Days to Decision
73 days
Submission Type
Statement