LIAISON RUBELLA IGM, LIAISON CONTROL RUBELLA IGM— 510(k) K122397
Substantially EquivalentDiaSorin, Inc.
FDA 510(k) clearance K122397 for LIAISON RUBELLA IGM, LIAISON CONTROL RUBELLA IGM, Substantially Equivalent on 2012-09-06. Applicant: DiaSorin, Inc.. Device class: 2.
Clearance details
- Applicant
- DiaSorin, Inc.
- Product code
- Code LFX
- Device class
- Class 2
- Regulation
- 21 CFR 866.3510
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Stillwater, MN, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.