ELEKTA NEUROMAG WITH MAXWELL FILTER
K-Number: K050035 · 2005-01-25
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Device Summary
Frequently Asked Questions
What is the ELEKTA NEUROMAG WITH MAXWELL FILTER?
ELEKTA NEUROMAG WITH MAXWELL FILTER is a medical device that received FDA 510(k) clearance on 2005-01-25. The listed applicant is Elekta Neuromag OY. The 510(k) number is K050035.
When did ELEKTA NEUROMAG WITH MAXWELL FILTER receive FDA 510(k) clearance?
ELEKTA NEUROMAG WITH MAXWELL FILTER received FDA 510(k) clearance on 2005-01-25, under 510(k) number K050035.
Who is the listed applicant for ELEKTA NEUROMAG WITH MAXWELL FILTER?
The FDA 510(k) record lists Elekta Neuromag OY as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ELEKTA NEUROMAG WITH MAXWELL FILTER?
The FDA product code for ELEKTA NEUROMAG WITH MAXWELL FILTER is OLX.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Elekta Neuromag OY as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: OLX)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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