VIS-1000 VIDEO SYSTEM— 510(k) K843806

Substantially Equivalent

Vistek Corp.

FDA 510(k) clearance K843806 for VIS-1000 VIDEO SYSTEM, Substantially Equivalent on 1984-12-12. Applicant: Vistek Corp.. Device class: 1.

Clearance details

Applicant: Vistek Corp.
Product code: Code KQM
Device class: Class 1
Regulation: 21 CFR 878.4160
Advisory panel: General, Plastic Surgery
Date received: 1984-09-27
Decision date: 1984-12-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Vistek Corp.

K904681 — VLS 5300 300W XENON LIGHT SOURCE1990-12-18
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K871034 — LCA 20001987-04-10
K860173 — VIS-2000 VIDEO SYSTEM1986-02-07

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