STERISIL ANTIMICROBIAL TUBING AND BOTTLE— 510(k) K031681

Name: FDA 510(k) clearance K031681
Creator: U.S. Food and Drug Administration
Published: 2003-10-30

Substantially Equivalent

Sterisil

FDA 510(k) clearance K031681 for STERISIL ANTIMICROBIAL TUBING AND BOTTLE, Substantially Equivalent on 2003-10-30. Applicant: Sterisil. Device class: 1.

Clearance details

Applicant: Sterisil
Product code: Code EIA
Device class: Class 1
Regulation: 21 CFR 872.6640
Advisory panel: Dental
Date received: 2003-05-30
Decision date: 2003-10-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Castle Rock, CO, US

Download summary PDF View on FDA.gov ↗

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