Nexus Universal, Nexus Universal Chroma— 510(k) K151332

Name: FDA 510(k) clearance K151332
Creator: U.S. Food and Drug Administration
Published: 2015-08-17

Substantially Equivalent

Sybron Dental Specialties

FDA 510(k) clearance K151332 for Nexus Universal, Nexus Universal Chroma, Substantially Equivalent on 2015-08-17. Applicant: Sybron Dental Specialties. Device class: 2.

Clearance details

Applicant: Sybron Dental Specialties
Product code: Code EMA
Device class: Class 2
Regulation: 21 CFR 872.3275
Advisory panel: Dental
Date received: 2015-05-19
Decision date: 2015-08-17
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Orange, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.