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FDA 510(k), K173119, DRI OCT Triton
FDA 510(k), K173119, DRI OCT Triton
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$149.00 USD
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510(K) Number: K173119
Device Name: DRI OCT Triton
Manufacturer: Topcon Corporation
Device Classification Name: Tomography, Optical Coherence
Regulation Number: 886.1570
Classification Product Code: OBO
Date Received: 09/29/2017
Decision Date: 01/19/2018
Regulation Medical Specialty: Ophthalmic
Device Name: DRI OCT Triton
Manufacturer: Topcon Corporation
Device Classification Name: Tomography, Optical Coherence
Regulation Number: 886.1570
Classification Product Code: OBO
Date Received: 09/29/2017
Decision Date: 01/19/2018
Regulation Medical Specialty: Ophthalmic
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- 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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