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OPTISCAN MODEL OPTISCAN CEIS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093624
510(k) Type
Traditional
Applicant
OPTISCAN PTY LTD.
Country
Australia
FDA Decision
Substantially Equivalent
Decision Date
3/5/2010
Days to Decision
102 days
Submission Type
Summary