RUBELLA IGG ELISA TEST— 510(k) K901635
Substantially EquivalentGull Laboratories, Inc.
FDA 510(k) clearance K901635 for RUBELLA IGG ELISA TEST, Substantially Equivalent on 1990-06-28. Applicant: Gull Laboratories, Inc..
Clearance details
- Applicant
- Gull Laboratories, Inc.
- Product code
- Code LFX
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Salt Lake City, UT, US
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