STERILOX LIQUID CHEMICAL STERILANT SYSTEM— 510(k) K063159

Substantially Equivalent

Puricore, Inc.

FDA 510(k) clearance K063159 for STERILOX LIQUID CHEMICAL STERILANT SYSTEM, Substantially Equivalent on 2007-04-02. Applicant: Puricore, Inc..

Clearance details

Applicant: Puricore, Inc.
Product code: Code MED
Advisory panel: General Hospital
Date received: 2006-10-17
Decision date: 2007-04-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Radnor, PA, US

Download summary PDF View on FDA.gov ↗

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