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FDA 510(k), K161461, BostonSight PD Prosthetic Device
FDA 510(k), K161461, BostonSight PD Prosthetic Device
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$149.00 USD
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510(K) Number: K161461
Device Name: BostonSight PD Prosthetic Device
Manufacturer: BostonSight
Device Classification Name: Lens, Contact (Other Material) - Daily
Regulation Number: 886.5916
Classification Product Code: HQD
Date Received: 05/26/2016
Decision Date: 07/25/2016
Regulation Medical Specialty: Ophthalmic
Device Name: BostonSight PD Prosthetic Device
Manufacturer: BostonSight
Device Classification Name: Lens, Contact (Other Material) - Daily
Regulation Number: 886.5916
Classification Product Code: HQD
Date Received: 05/26/2016
Decision Date: 07/25/2016
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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