BIOPLEX 2200 ANA SCREEN WITH MEDICAL DECISION SUPPORT SOFTWARE FOR USE WITH BIOPLEX 2200 MULTI-ANALYTE DETECTION SYSTEM— 510(k) K043341
Substantially EquivalentBio-Rad Laboratories, Inc.
FDA 510(k) clearance K043341 for BIOPLEX 2200 ANA SCREEN WITH MEDICAL DECISION SUPPORT SOFTWARE FOR USE WITH BIOPLEX 2200 MULTI-ANALYTE DETECTION SYSTEM, Substantially Equivalent on 2005-10-27. Applicant: Bio-Rad Laboratories, Inc..
Clearance details
- Applicant
- Bio-Rad Laboratories, Inc.
- Product code
- Code NVI
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Redmond, WA, US
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