GLIADIN IGG ELISA TEST SYSTEM— 510(k) K990204
Substantially EquivalentZeus Scientific, Inc.
FDA 510(k) clearance K990204 for GLIADIN IGG ELISA TEST SYSTEM, Substantially Equivalent on 1999-03-26. Applicant: Zeus Scientific, Inc.. Device class: 2.
Clearance details
- Applicant
- Zeus Scientific, Inc.
- Product code
- Code MST
- Device class
- Class 2
- Regulation
- 21 CFR 866.5750
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Raritan, NJ, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.