700 SERIES BIOMAGNETOMETER— 510(k) K901215

Name: FDA 510(k) clearance K901215
Creator: U.S. Food and Drug Administration
Published: 1990-06-25

Substantially Equivalent

Biomagnetic Technologies, Inc.

FDA 510(k) clearance K901215 for 700 SERIES BIOMAGNETOMETER, Substantially Equivalent on 1990-06-25. Applicant: Biomagnetic Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Biomagnetic Technologies, Inc.
Product code: Code OLX
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 1990-03-14
Decision date: 1990-06-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.