STERIS RESERT XL TEST STRIP— 510(k) K081600
Substantially EquivalentSTERIS Corporation
FDA 510(k) clearance K081600 for STERIS RESERT XL TEST STRIP, Substantially Equivalent on 2008-08-22. Applicant: STERIS Corporation.
Clearance details
- Applicant
- STERIS Corporation
- Product code
- Code JOJ
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mentor, OH, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.