Last synced on 25 January 2026 at 3:41 am

OTI-SCAN 3000

Page Type
Cleared 510(K)
PDF
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
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