NEUROTRAC II— 510(k) K914571

Substantially Equivalent

Moberg Medical, Inc.

FDA 510(k) clearance K914571 for NEUROTRAC II, Substantially Equivalent on 1992-01-30. Applicant: Moberg Medical, Inc.. Device class: 2.

Clearance details

Applicant: Moberg Medical, Inc.
Product code: Code GWQ
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 1991-10-15
Decision date: 1992-01-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ambler, PA, US

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