Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ELEKTA NEUROMAG WITH MAXFILTER

K-Number: K091393 · 2010-10-26

Decision Date2010-10-26
Product CodeOLX
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELEKTA NEUROMAG WITH MAXFILTER is the device name listed in this FDA 510(k) record. The listed applicant is Elekta Neuromag OY. It received FDA 510(k) clearance on 2010-10-26 under 510(k) number K091393. The device is classified under product code OLX. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELEKTA NEUROMAG WITH MAXFILTER?

ELEKTA NEUROMAG WITH MAXFILTER is a medical device that received FDA 510(k) clearance on 2010-10-26. The listed applicant is Elekta Neuromag OY. The 510(k) number is K091393.

When did ELEKTA NEUROMAG WITH MAXFILTER receive FDA 510(k) clearance?

ELEKTA NEUROMAG WITH MAXFILTER received FDA 510(k) clearance on 2010-10-26, under 510(k) number K091393.

Who is the listed applicant for ELEKTA NEUROMAG WITH MAXFILTER?

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 MAXFILTER?

The FDA product code for ELEKTA NEUROMAG WITH MAXFILTER 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.

↑