NEXUS 2 MODIFIED— 510(k) K013008

Name: FDA 510(k) clearance K013008
Creator: U.S. Food and Drug Administration
Published: 2001-10-02

Substantially Equivalent

Sybron Dental Specialties, Inc.

FDA 510(k) clearance K013008 for NEXUS 2 MODIFIED, Substantially Equivalent on 2001-10-02. Applicant: Sybron Dental Specialties, Inc.. Device class: 2.

Clearance details

Applicant: Sybron Dental Specialties, Inc.
Product code: Product code EMA
Device class: Class 2
Regulation: 21 CFR 872.3275
Advisory panel: Dental
Date received: 2001-09-06
Decision date: 2001-10-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Orange, CA, US

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