FDA 510(k), K093520, VIVOSIGHT TOPICAL OCT SYSTEM

FDA 510(k), K093520, VIVOSIGHT TOPICAL OCT SYSTEM

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510(K) Number: K093520
Device Name: VIVOSIGHT TOPICAL OCT SYSTEM
Manufacturer: MARTIN JOHNS
Device Classification Name: System, Imaging, Optical Coherence Tomography (Oct)
Regulation Number: NQQ
Classification Product Code: 11/13/2009
Date Received: 01/05/2010
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery

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