CEDIA SIROLIMUS ASSAY— 510(k) DEN040008
UnknownMicrogenics Corp.
FDA 510(k) clearance DEN040008 for CEDIA SIROLIMUS ASSAY, Unknown on 2004-07-28. Applicant: Microgenics Corp.. Device class: 2.
Clearance details
- Applicant
- Microgenics Corp.
- Product code
- Code NRP
- Device class
- Class 2
- Regulation
- 21 CFR 862.3840
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Post-NSE
- Location
- Fremont Blvd., CA, US
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