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OTI-SCAN 3000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092837
510(k) Type
Special
Applicant
OPKO INSTRUMENTATION, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/2009
Days to Decision
99 days
Submission Type
Statement

OTI-SCAN 3000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092837
510(k) Type
Special
Applicant
OPKO INSTRUMENTATION, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/2009
Days to Decision
99 days
Submission Type
Statement