INTEGRA REAGENT CASSETTE FOR APOLIPOPROTEIN B
FDA 510(k) clearance K990595 · decided 1999-04-14
Clearance details
- K-number
- K990595
- Device name
- INTEGRA REAGENT CASSETTE FOR APOLIPOPROTEIN B
- Applicant
- Roche Diagnostics Corp.
- Decision
- Substantially Equivalent
- Date received
- 1999-02-24
- Decision date
- 1999-04-14
- Days to decision
- 49 days
- Clearance type
- Traditional
- Product code
- DFC
- Device class
- 2
- Regulation number
- 866.5600
- 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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