FIDIS CELIAC— 510(k) K041002
Substantially EquivalentBiomedical Diagnostics S.A.
FDA 510(k) clearance K041002 for FIDIS CELIAC, Substantially Equivalent on 2004-09-24. Applicant: Biomedical Diagnostics S.A.. Device class: 2.
Clearance details
- Applicant
- Biomedical Diagnostics S.A.
- 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
- Marne-La-Vallee, Cedex 2, FR
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Data sourced from openFDA. This site is unofficial and independent of the FDA.