ELEKTA OY— 510(k) K041264

Substantially Equivalent

Elekta Neuromag OY

FDA 510(k) clearance K041264 for ELEKTA OY, Substantially Equivalent on 2004-08-10. Applicant: Elekta Neuromag OY. Device class: 2.

Clearance details

Applicant: Elekta Neuromag OY
Product code: Code OLX
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 2004-05-12
Decision date: 2004-08-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Helsinki, FI

Download summary PDF View on FDA.gov ↗

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More clearances from Elekta Neuromag OY

K091393 — ELEKTA NEUROMAG WITH MAXFILTER2010-10-26
K081430 — ELEKTA NEUROMAG WITH MAXWELL FILTER WITH INTERNAL ACTIVE SHIELDING2008-07-28
K050035 — ELEKTA NEUROMAG WITH MAXWELL FILTER2005-01-25

Data sourced from openFDA. This site is unofficial and independent of the FDA.