EIA RUBELLA-G— 510(k) K802339
Substantially EquivalentBeckman Instruments, Inc.
FDA 510(k) clearance K802339 for EIA RUBELLA-G, Substantially Equivalent on 1980-12-18. Applicant: Beckman Instruments, Inc.. Device class: 2.
Clearance details
- Applicant
- Beckman Instruments, Inc.
- Product code
- Code GOL
- Device class
- Class 2
- Regulation
- 21 CFR 866.3510
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.