RIDASCREEN NOROVIRUS 3RD GENERATION EIA— 510(k) DEN110001
UnknownR-Biopharm AG
FDA 510(k) clearance DEN110001 for RIDASCREEN NOROVIRUS 3RD GENERATION EIA, Unknown on 2011-02-23. Applicant: R-Biopharm AG. Device class: 2.
Clearance details
- Applicant
- R-Biopharm AG
- Product code
- Code OUC
- Device class
- Class 2
- Regulation
- 21 CFR 866.3395
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Post-NSE
- Location
- East Stroudsburg, PA, US
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