PAS ALCOVISOR MARS, PAS ALCOVISOR SATELLITE— 510(k) K123470

Name: FDA 510(k) clearance K123470
Creator: U.S. Food and Drug Administration
Published: 2013-04-29

Substantially Equivalent

Pas Systems International, Inc.

FDA 510(k) clearance K123470 for PAS ALCOVISOR MARS, PAS ALCOVISOR SATELLITE, Substantially Equivalent on 2013-04-29. Applicant: Pas Systems International, Inc.. Device class: 1.

Clearance details

Applicant: Pas Systems International, Inc.
Product code: Code DJZ
Device class: Class 1
Regulation: 21 CFR 862.3050
Advisory panel: Clinical Toxicology
Date received: 2012-11-13
Decision date: 2013-04-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fredericksburg, VA, US

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