FDA 510(k), K062416, RETINAL FUNCTIONAL IMAGER (RFI)
FDA 510(k), K062416, RETINAL FUNCTIONAL IMAGER (RFI)
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510(K) Number: K062416
Device Name: RETINAL FUNCTIONAL IMAGER (RFI)
Manufacturer: OPTICAL IMAGING LTD.
Device Classification Name: camera, ophthalmic, ac-powered
Regulation Number: 886.1120
Classification Product Code: HKI
Date Received: 08/17/2006
Decision Date: 11/17/2006
Regulation Medical Specialty: Ophthalmic
Device Name: RETINAL FUNCTIONAL IMAGER (RFI)
Manufacturer: OPTICAL IMAGING LTD.
Device Classification Name: camera, ophthalmic, ac-powered
Regulation Number: 886.1120
Classification Product Code: HKI
Date Received: 08/17/2006
Decision Date: 11/17/2006
Regulation Medical Specialty: Ophthalmic
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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