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FDA 510(k), K013110, ANISEIKONIA INSPECTOR
FDA 510(k), K013110, ANISEIKONIA INSPECTOR
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510(K) Number: K013110
Device Name: ANISEIKONIA INSPECTOR
Manufacturer: OPTICAL DIAGNOSTICS, INC.
Device Classification Name: haploscope
Regulation Number: 886.1340
Classification Product Code: HJT
Date Received: 07/11/2001
Decision Date: 12/19/2001
Regulation Medical Specialty: Ophthalmic
Device Name: ANISEIKONIA INSPECTOR
Manufacturer: OPTICAL DIAGNOSTICS, INC.
Device Classification Name: haploscope
Regulation Number: 886.1340
Classification Product Code: HJT
Date Received: 07/11/2001
Decision Date: 12/19/2001
Regulation Medical Specialty: Ophthalmic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. IMPORTANT: The FDA FOIA office operations are currently suspended. We are happy to make the request but do not know when we will receive a response. Learn more about Fast-Track Requests here.
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