TINA-QUANT MYOGLOBIN GEN.2 TEST SYSTEM
FDA 510(k) clearance K061683 · decided 2006-07-21
Clearance details
- K-number
- K061683
- Device name
- TINA-QUANT MYOGLOBIN GEN.2 TEST SYSTEM
- Applicant
- Roche Diagnostics Corp.
- Decision
- Substantially Equivalent
- Date received
- 2006-06-15
- Decision date
- 2006-07-21
- Days to decision
- 36 days
- Clearance type
- Traditional
- Product code
- DDR
- Device class
- 2
- Regulation number
- 866.5680
- Medical specialty
- Immunology
- Advisory committee
- Immunology
- Location
- Indianapolis, IN, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.
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