NEUROMAG-122— 510(k) K962764

Name: FDA 510(k) clearance K962764
Creator: U.S. Food and Drug Administration
Published: 1996-10-31

Substantially Equivalent

Philips Medical Systems (Cleveland), Inc.

FDA 510(k) clearance K962764 for NEUROMAG-122, Substantially Equivalent on 1996-10-31. Applicant: Philips Medical Systems (Cleveland), Inc.. Device class: 2.

Clearance details

Applicant: Philips Medical Systems (Cleveland), Inc.
Product code: Code OLY
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 1996-07-16
Decision date: 1996-10-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Highland Heights, OH, US

Download summary PDF View on FDA.gov ↗

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