DURABLUE STERILIZATION WRAP
FDA 510(k) clearance K123857 · decided 2013-01-23
Clearance details
- K-number
- K123857
- Device name
- DURABLUE STERILIZATION WRAP
- Applicant
- Cardinal Health200, LLC
- Decision
- Substantially Equivalent
- Date received
- 2012-12-14
- Decision date
- 2013-01-23
- Days to decision
- 40 days
- Clearance type
- Traditional
- Product code
- FRG
- Device class
- 2
- Regulation number
- 880.6850
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Waukegan, IL, US
- Third-party review
- Yes
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.