DAN KERRISON RONGEURS, MODELS K1 + BILLY 1— 510(k) K023868

Name: FDA 510(k) clearance K023868
Creator: U.S. Food and Drug Administration
Published: 2003-02-07

Substantially Equivalent

Dannoritzer Medical Instruments

FDA 510(k) clearance K023868 for DAN KERRISON RONGEURS, MODELS K1 + BILLY 1, Substantially Equivalent on 2003-02-07. Applicant: Dannoritzer Medical Instruments. Device class: 2.

Clearance details

Applicant: Dannoritzer Medical Instruments
Product code: Code HAE
Device class: Class 2
Regulation: 21 CFR 882.4840
Advisory panel: Neurology
Date received: 2002-11-20
Decision date: 2003-02-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hot Springs, NC, US

Download summary PDF View on FDA.gov ↗

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