STERILOX LIQUID CHEMICAL STERILANT SYSTEM— 510(k) K063159
Substantially EquivalentPuricore, Inc.
FDA 510(k) clearance K063159 for STERILOX LIQUID CHEMICAL STERILANT SYSTEM, Substantially Equivalent on 2007-04-02. Applicant: Puricore, Inc.. Device class: 2.
Clearance details
- Applicant
- Puricore, Inc.
- Product code
- Code MED
- Device class
- Class 2
- Regulation
- 21 CFR 880.6885
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Radnor, PA, US
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