VIOTEC V-2200 ULTRAVIOLET GERMICIDAL AIR PURIFICATION SYSTEM— 510(k) K954448

Name: FDA 510(k) clearance K954448
Creator: U.S. Food and Drug Administration
Published: 1996-10-28

Substantially Equivalent

Schiff & Co.

FDA 510(k) clearance K954448 for VIOTEC V-2200 ULTRAVIOLET GERMICIDAL AIR PURIFICATION SYSTEM, Substantially Equivalent on 1996-10-28. Applicant: Schiff & Co.. Device class: 2.

Clearance details

Applicant: Schiff & Co.
Product code: Code FRA
Device class: Class 2
Regulation: 21 CFR 880.6500
Advisory panel: General Hospital
Date received: 1995-09-25
Decision date: 1996-10-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Cadwell, NJ, US

Download summary PDF View on FDA.gov ↗

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