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FDA 510(k), K080043, VIZILITE EYEWEAR
FDA 510(k), K080043, VIZILITE EYEWEAR
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510(K) Number: K080043
Device Name: VIZILITE EYEWEAR
Manufacturer: MARK BRIDE
Device Classification Name: Diagnostic Light, Soft Tissue Detector
Regulation Number: NXV
Classification Product Code: KXA
Date Received: 01/08/2008
Decision Date: 04/04/2008
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental
Device Name: VIZILITE EYEWEAR
Manufacturer: MARK BRIDE
Device Classification Name: Diagnostic Light, Soft Tissue Detector
Regulation Number: NXV
Classification Product Code: KXA
Date Received: 01/08/2008
Decision Date: 04/04/2008
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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