NEUROMAG VECTORVIEW— 510(k) K984401

Name: FDA 510(k) clearance K984401
Creator: U.S. Food and Drug Administration
Published: 1998-12-30

Substantially Equivalent

Philips Medical Systems (Cleveland), Inc.

FDA 510(k) clearance K984401 for NEUROMAG VECTORVIEW, Substantially Equivalent on 1998-12-30. Applicant: Philips Medical Systems (Cleveland), Inc.. Device class: 2.

Clearance details

Applicant: Philips Medical Systems (Cleveland), Inc.
Product code: Code OLX
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 1998-12-09
Decision date: 1998-12-30
Decision: Substantially Equivalent
Clearance type: Special
Location: Cleveland, OH, 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.