VIOTEC S-4000-CR SECURITY SERIES ULTRAVIOLET GERMICIDAL AIR PURIFICATION SYSTEM— 510(k) K960833

Name: FDA 510(k) clearance K960833
Creator: U.S. Food and Drug Administration
Published: 1996-07-25

Substantially Equivalent

Uv Technologies, Inc.

FDA 510(k) clearance K960833 for VIOTEC S-4000-CR SECURITY SERIES ULTRAVIOLET GERMICIDAL AIR PURIFICATION SYSTEM, Substantially Equivalent on 1996-07-25. Applicant: Uv Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Uv Technologies, Inc.
Product code: Code FRA
Device class: Class 2
Regulation: 21 CFR 880.6500
Advisory panel: General Hospital
Date received: 1996-02-29
Decision date: 1996-07-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Cadwell, NJ, US

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