HERPES VIRUS HOMINIS ANTIBODY TEST SYS.— 510(k) K812085
Substantially EquivalentZeus Scientific, Inc.
FDA 510(k) clearance K812085 for HERPES VIRUS HOMINIS ANTIBODY TEST SYS., Substantially Equivalent on 1981-09-01. Applicant: Zeus Scientific, Inc.. Device class: 2.
Clearance details
- Applicant
- Zeus Scientific, Inc.
- Product code
- Code GQL
- Device class
- Class 2
- Regulation
- 21 CFR 866.3305
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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