NEUROTRAIN— 510(k) K883896

Substantially Equivalent

Sterne Equipment Co., Ltd.

FDA 510(k) clearance K883896 for NEUROTRAIN, Substantially Equivalent on 1989-07-14. Applicant: Sterne Equipment Co., Ltd.. Device class: 2.

Clearance details

Applicant: Sterne Equipment Co., Ltd.
Product code: Code LIH
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1988-09-14
Decision date: 1989-07-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brampton, On., CA

Download summary PDF View on FDA.gov ↗

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More clearances from Sterne Equipment Co., Ltd.

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K970155 — NEURO-TRAIN II (2)1997-03-17
K931279 — ACU-RAY1993-11-03

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