Last synced on 4 February 2023 at 10:33 pm

RETINA TESTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914393
510(k) Type
Traditional
Applicant
RETINA TESTER
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/1992
Days to Decision
153 days
Submission Type
Statement

RETINA TESTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914393
510(k) Type
Traditional
Applicant
RETINA TESTER
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/1992
Days to Decision
153 days
Submission Type
Statement