ULTRA-LINE RONGEUR— 510(k) K943635

Substantially Equivalent

V. Mueller Neuro/Spine

FDA 510(k) clearance K943635 for ULTRA-LINE RONGEUR, Substantially Equivalent on 1994-12-07. Applicant: V. Mueller Neuro/Spine. Device class: 2.

Clearance details

Applicant: V. Mueller Neuro/Spine
Product code: Code HAE
Device class: Class 2
Regulation: 21 CFR 882.4840
Advisory panel: Neurology
Date received: 1994-07-27
Decision date: 1994-12-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Carlos, 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.