VTS-1000 VISUAL TESTING SYSTEM— 510(k) K812331

Name: FDA 510(k) clearance K812331
Creator: U.S. Food and Drug Administration
Published: 1981-11-16

Substantially Equivalent

Nicolet Biomedical Instruments

FDA 510(k) clearance K812331 for VTS-1000 VISUAL TESTING SYSTEM, Substantially Equivalent on 1981-11-16. Applicant: Nicolet Biomedical Instruments. Device class: 2.

Clearance details

Applicant: Nicolet Biomedical Instruments
Product code: Code HLX
Device class: Class 2
Regulation: 21 CFR 886.1630
Advisory panel: Ophthalmic
Date received: 1981-08-18
Decision date: 1981-11-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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