STERILOX LIQUID CHEMICAL STERILANT SYSTEM— 510(k) K013280
Substantially EquivalentSterilox Technologies, Inc.
FDA 510(k) clearance K013280 for STERILOX LIQUID CHEMICAL STERILANT SYSTEM, Substantially Equivalent on 2002-09-18. Applicant: Sterilox Technologies, Inc.. Device class: 2.
Clearance details
- Applicant
- Sterilox Technologies, 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
- Yardley, PA, US
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