FDA 510(k), K201005, FullFocus

FDA 510(k), K201005, FullFocus

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510(K) Number: K201005
Device Name: FullFocus
Manufacturer: Jillian Sue
Device Classification Name: Digital Pathology Image Viewing And Management Software
Regulation Number: QKQ
Classification Product Code: 04/16/2020
Date Received: 07/15/2020
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Pathology

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