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FDA 510(k)

MODIFIED BRAIN ATLAS III

K-Number: K854362 · 1986-04-22

ApplicantBio-Logic Systems Corp.
Decision Date1986-04-22
Product CodeGWE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MODIFIED BRAIN ATLAS III is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Logic Systems Corp.. It received FDA 510(k) clearance on 1986-04-22 under 510(k) number K854362. The device is classified under product code GWE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED BRAIN ATLAS III?

MODIFIED BRAIN ATLAS III is a medical device that received FDA 510(k) clearance on 1986-04-22. The listed applicant is Bio-Logic Systems Corp.. The 510(k) number is K854362.

When did MODIFIED BRAIN ATLAS III receive FDA 510(k) clearance?

MODIFIED BRAIN ATLAS III received FDA 510(k) clearance on 1986-04-22, under 510(k) number K854362.

Who is the listed applicant for MODIFIED BRAIN ATLAS III?

The FDA 510(k) record lists Bio-Logic Systems Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED BRAIN ATLAS III?

The FDA product code for MODIFIED BRAIN ATLAS III is GWE.

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Related Devices (Code: GWE)

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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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