FDA 510(k), K081960, INVISALIGN SYSTEM
FDA 510(k), K081960, INVISALIGN SYSTEM
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510(K) Number: K081960
Device Name: INVISALIGN SYSTEM
Manufacturer:
Device Classification Name: Aligner, Sequential
Regulation Number: 872.5470
Classification Product Code: NXC
Date Received: 07/09/2008
Decision Date: 12/17/2008
Regulation Medical Specialty: Dental
Device Name: INVISALIGN SYSTEM
Manufacturer:
Device Classification Name: Aligner, Sequential
Regulation Number: 872.5470
Classification Product Code: NXC
Date Received: 07/09/2008
Decision Date: 12/17/2008
Regulation Medical Specialty: Dental