UV AIR STERILIGHT— 510(k) K884579

Name: FDA 510(k) clearance K884579
Creator: U.S. Food and Drug Administration
Published: 1988-12-12

Substantially Equivalent

Allseasons Environmental Control, Inc.

FDA 510(k) clearance K884579 for UV AIR STERILIGHT, Substantially Equivalent on 1988-12-12. Applicant: Allseasons Environmental Control, Inc.. Device class: 2.

Clearance details

Applicant: Allseasons Environmental Control, Inc.
Product code: Code FRA
Device class: Class 2
Regulation: 21 CFR 880.6500
Advisory panel: General Hospital
Date received: 1988-11-03
Decision date: 1988-12-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: London, Ontario, CA

Download summary PDF View on FDA.gov ↗

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