VENTRE/ZYME IGE KIT— 510(k) K831485
Substantially EquivalentVentrex Laboratories, Inc.
FDA 510(k) clearance K831485 for VENTRE/ZYME IGE KIT, Substantially Equivalent on 1983-06-02. Applicant: Ventrex Laboratories, Inc.. Device class: 2.
Clearance details
- Applicant
- Ventrex Laboratories, Inc.
- Product code
- Code DGC
- Device class
- Class 2
- Regulation
- 21 CFR 866.5510
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
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