NEDBOND EJECTOR KERRISON RONGEUR— 510(k) K933978

Name: FDA 510(k) clearance K933978
Creator: U.S. Food and Drug Administration
Published: 1994-01-12

Substantially Equivalent

Redmond Neurotechnologies Corp.

FDA 510(k) clearance K933978 for NEDBOND EJECTOR KERRISON RONGEUR, Substantially Equivalent on 1994-01-12. Applicant: Redmond Neurotechnologies Corp.. Device class: 2.

Clearance details

Applicant: Redmond Neurotechnologies Corp.
Product code: Code HAE
Device class: Class 2
Regulation: 21 CFR 882.4840
Advisory panel: Neurology
Date received: 1993-08-16
Decision date: 1994-01-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Zurich, IL, 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.