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REICHERT CT200 CONTACT TONOMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000288
510(k) Type
Traditional
Applicant
REICHERT OPHTHALMIC INSTRUMENTS, DIV. LEICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/2000
Days to Decision
52 days
Submission Type
Statement

REICHERT CT200 CONTACT TONOMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000288
510(k) Type
Traditional
Applicant
REICHERT OPHTHALMIC INSTRUMENTS, DIV. LEICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/2000
Days to Decision
52 days
Submission Type
Statement