IGG ANTI-ATHEROX TEST KIT— 510(k) K072032
Substantially EquivalentCorgenix, Inc.
FDA 510(k) clearance K072032 for IGG ANTI-ATHEROX TEST KIT, Substantially Equivalent on 2008-04-04. Applicant: Corgenix, Inc.. Device class: 2.
Clearance details
- Applicant
- Corgenix, Inc.
- Product code
- Code MSV
- Device class
- Class 2
- Regulation
- 21 CFR 866.5660
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Broomfield, CO, US
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