VARICELLA-ZOSTER VIRUS ANTIBODY TEST KIT-LATEX AGG— 510(k) K903882
Substantially EquivalentViral Antigens, Inc.
FDA 510(k) clearance K903882 for VARICELLA-ZOSTER VIRUS ANTIBODY TEST KIT-LATEX AGG, Substantially Equivalent on 1990-12-04. Applicant: Viral Antigens, Inc.. Device class: 2.
Clearance details
- Applicant
- Viral Antigens, Inc.
- Product code
- Code GQW
- Device class
- Class 2
- Regulation
- 21 CFR 866.3900
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Memphis, TN, US
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