IMMULITE RUBELLA IGG— 510(k) K963613
Substantially EquivalentDiagnostic Products Corp.
FDA 510(k) clearance K963613 for IMMULITE RUBELLA IGG, Substantially Equivalent on 1997-04-02. Applicant: Diagnostic Products Corp.. Device class: 2.
Clearance details
- Applicant
- Diagnostic Products Corp.
- 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
- Los Angeles, CA, US
Recent devices under product code LFX
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Data sourced from openFDA. This site is unofficial and independent of the FDA.