SOMATOSENSORY STIMULUS SYSTEM— 510(k) K913604

Name: FDA 510(k) clearance K913604
Creator: U.S. Food and Drug Administration
Published: 1991-12-09

Substantially Equivalent

Biomagnetic Technologies, Inc.

FDA 510(k) clearance K913604 for SOMATOSENSORY STIMULUS SYSTEM, Substantially Equivalent on 1991-12-09. Applicant: Biomagnetic Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Biomagnetic Technologies, Inc.
Product code: Code GZP
Device class: Class 2
Regulation: 21 CFR 882.1880
Advisory panel: Neurology
Date received: 1991-08-14
Decision date: 1991-12-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

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