MODIFIED LABSYSTEMS' RUBELLA IGG EIA TEST KIT— 510(k) K890091
Substantially EquivalentLabsystems, Inc.
FDA 510(k) clearance K890091 for MODIFIED LABSYSTEMS' RUBELLA IGG EIA TEST KIT, Substantially Equivalent on 1989-02-03. Applicant: Labsystems, Inc..
Clearance details
- Applicant
- Labsystems, Inc.
- Product code
- Code LFX
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Finland, FI
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