VERIFY CHALLENGE PACKS - VERSION 2
FDA 510(k) clearance K073683 · decided 2008-01-25
Clearance details
- K-number
- K073683
- Device name
- VERIFY CHALLENGE PACKS - VERSION 2
- Applicant
- STERIS Corporation
- Decision
- Substantially Equivalent
- Date received
- 2007-12-28
- Decision date
- 2008-01-25
- Days to decision
- 28 days
- Clearance type
- Special
- Product code
- JOJ
- Device class
- 2
- Regulation number
- 880.2800
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Mentor, OH, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.