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OIS EYESCAN PORTABLE MODULAR IMAGING SYSTEM, MODEL OIS EYESCAN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092374
510(k) Type
Traditional
Applicant
OPHTHALMIC IMAGING SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2009
Days to Decision
104 days
Submission Type
Summary

OIS EYESCAN PORTABLE MODULAR IMAGING SYSTEM, MODEL OIS EYESCAN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092374
510(k) Type
Traditional
Applicant
OPHTHALMIC IMAGING SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2009
Days to Decision
104 days
Submission Type
Summary