MAGNES 2500 WH BIOMAGNETOMETER— 510(k) K962317

Name: FDA 510(k) clearance K962317
Creator: U.S. Food and Drug Administration
Published: 1997-05-07

Substantially Equivalent

Biomagnetic Technologies, Inc.

FDA 510(k) clearance K962317 for MAGNES 2500 WH BIOMAGNETOMETER, Substantially Equivalent on 1997-05-07. Applicant: Biomagnetic Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Biomagnetic Technologies, Inc.
Product code: Code OLY
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 1996-06-17
Decision date: 1997-05-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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