VISUALAX— 510(k) K781634

Substantially Equivalent

Farrall Instruments, Inc.

FDA 510(k) clearance K781634 for VISUALAX, Substantially Equivalent on 1978-10-03. Applicant: Farrall Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Farrall Instruments, Inc.
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 1978-09-22
Decision date: 1978-10-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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