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NON-CONTACT TONOMETERS, OCULAR RESPONSE ANALYZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032799
510(k) Type
Traditional
Applicant
REICHERT INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/2004
Days to Decision
133 days
Submission Type
Statement

NON-CONTACT TONOMETERS, OCULAR RESPONSE ANALYZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032799
510(k) Type
Traditional
Applicant
REICHERT INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/2004
Days to Decision
133 days
Submission Type
Statement