SIEGEN VISUAL STIMULATOR— 510(k) K844616

Substantially Equivalent

Siegen Corp.

FDA 510(k) clearance K844616 for SIEGEN VISUAL STIMULATOR, Substantially Equivalent on 1985-02-14. Applicant: Siegen Corp.. Device class: 2.

Clearance details

Applicant: Siegen Corp.
Product code: Code GWE
Device class: Class 2
Regulation: 21 CFR 882.1890
Advisory panel: Neurology
Date received: 1984-11-27
Decision date: 1985-02-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mountain View, CA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Siegen Corp.

K871964 — SIEGEN NEUROSCOPE SEEG FOR EVOKED RESPONSE STIMU.1987-10-01
K861884 — NEUROSCOPE SEEG1986-10-14
K862430 — SIEGEN HEADPHONES1986-09-26
K844646 — SIEGEN SURFACE ELECTRODES1984-12-11
K843464 — SIEGEN NEUROSCOPE1984-11-20

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