FDA 510(k) K993708, BIOMAGNETIC TECHNOLOGIES MAGNES 3600 WHOLE HEAD MEG, by Biomagnetic Technologies, Inc.

FDA 510(k) K993708, BIOMAGNETIC TECHNOLOGIES MAGNES 3600 WHOLE HEAD MEG, by Biomagnetic Technologies, Inc.

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Device Classification Name: Source Localization Software For Electroencephalograph Or Magnetoencephalograph
510(k) Number: K993708
Device Name: BIOMAGNETIC TECHNOLOGIES MAGNES 3600 WHOLE HEAD MEG
Applicant: Biomagnetic Technologies, Inc.
Regulation Number: 882.14
Classification Product Code: OLX
Date Received: 1999-11-03
Decision Date: 1999-12-03
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology
510k Review Panel: Neurology

Total number of pages: 153
Fully redacted pages: 9
Content pages: 144

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