DIAGNON FERRITIN 125 I RIA KIT— 510(k) K830580
Substantially EquivalentIagnon Corp.
FDA 510(k) clearance K830580 for DIAGNON FERRITIN 125 I RIA KIT, Substantially Equivalent on 1983-05-05. Applicant: Iagnon Corp.. Device class: 2.
Clearance details
- Applicant
- Iagnon Corp.
- Product code
- Code DBF
- Device class
- Class 2
- Regulation
- 21 CFR 866.5340
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.