NEUROLAB II— 510(k) K844481

Substantially Equivalent

Teca, Inc.

FDA 510(k) clearance K844481 for NEUROLAB II, Substantially Equivalent on 1985-05-20. Applicant: Teca, Inc.. Device class: 1.

Clearance details

Applicant: Teca, Inc.
Product code: Code GWS
Device class: Class 1
Regulation: 21 CFR 882.1420
Advisory panel: Neurology
Date received: 1984-11-19
Decision date: 1985-05-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pleasantiville, NY, US

Download summary PDF View on FDA.gov ↗

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More clearances from Teca, Inc.

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K896666 — P460, DG32 ELECTROENCEPHALOGRAPH1990-02-16
K894889 — TECA NEUROMAPPER 3861989-12-22

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