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FDA 510(k), K062074, IRIDEX WIRELESS FOOTSWITCH
FDA 510(k), K062074, IRIDEX WIRELESS FOOTSWITCH
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510(K) Number: K062074
Device Name: IRIDEX WIRELESS FOOTSWITCH
Manufacturer: JOHN JOSSY
Device Classification Name: Laser, Ophthalmic
Regulation Number: HQF
Classification Product Code: 07/21/2006
Date Received: 11/14/2006
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Ophthalmic
Device Name: IRIDEX WIRELESS FOOTSWITCH
Manufacturer: JOHN JOSSY
Device Classification Name: Laser, Ophthalmic
Regulation Number: HQF
Classification Product Code: 07/21/2006
Date Received: 11/14/2006
Decision Date: Substantially Equivalent (SESE)
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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