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FDA 510(k), K171295, ULab Systems Treatment Planning Software
FDA 510(k), K171295, ULab Systems Treatment Planning Software
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510(K) Number: K171295
Device Name: ULab Systems Treatment Planning Software
Manufacturer: ULab Systems, Inc.
Device Classification Name: orthodontic software
Regulation Number: 872.5470
Classification Product Code: PNN
Date Received: 05/02/2017
Decision Date: 01/09/2018
Regulation Medical Specialty: Dental
Device Name: ULab Systems Treatment Planning Software
Manufacturer: ULab Systems, Inc.
Device Classification Name: orthodontic software
Regulation Number: 872.5470
Classification Product Code: PNN
Date Received: 05/02/2017
Decision Date: 01/09/2018
Regulation Medical Specialty: Dental
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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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