DETECTAR, MODEL N123-MI— 510(k) K023367

Substantially Equivalent

Neks Technologies

FDA 510(k) clearance K023367 for DETECTAR, MODEL N123-MI, Substantially Equivalent on 2003-06-25. Applicant: Neks Technologies. Device class: 1.

Clearance details

Applicant: Neks Technologies
Product code: Code EJB
Device class: Class 1
Regulation: 21 CFR 872.4565
Advisory panel: Dental
Date received: 2002-10-08
Decision date: 2003-06-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chapel Hill, NC, 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.