MERIDIAN— 510(k) K131753

Substantially Equivalent

Ab Ardent

FDA 510(k) clearance K131753 for MERIDIAN, Substantially Equivalent on 2013-11-14. Applicant: Ab Ardent. Device class: 2.

Clearance details

Applicant: Ab Ardent
Product code: Code EBF
Device class: Class 2
Regulation: 21 CFR 872.3690
Advisory panel: Dental
Date received: 2013-06-14
Decision date: 2013-11-14
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Amherst, NY, US

Download summary PDF View on FDA.gov ↗

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