IT/IF CONTROL
FDA 510(k) clearance K101863 · decided 2011-11-07
Clearance details
- K-number
- K101863
- Device name
- IT/IF CONTROL
- Applicant
- Sebia
- Decision
- Substantially Equivalent
- Date received
- 2010-07-02
- Decision date
- 2011-11-07
- Days to decision
- 493 days
- Clearance type
- Traditional
- Product code
- JJY
- Device class
- 1
- Regulation number
- 862.1660
- Medical specialty
- Clinical Chemistry
- Advisory committee
- Clinical Chemistry
- Location
- Norcross, GA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.