MODIFICATION TO FIDIS VASCULITIS, MODEL MX007— 510(k) K070458
Substantially EquivalentBiomedical Diagnostics (Bmd) SA
FDA 510(k) clearance K070458 for MODIFICATION TO FIDIS VASCULITIS, MODEL MX007, Substantially Equivalent on 2007-12-21. Applicant: Biomedical Diagnostics (Bmd) SA. Device class: 2.
Clearance details
- Applicant
- Biomedical Diagnostics (Bmd) SA
- Product code
- Code MOB
- Device class
- Class 2
- Regulation
- 21 CFR 866.5660
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Marne La Vallee Cedex 2, FR
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More clearances from Biomedical Diagnostics (Bmd) SA
view allData sourced from openFDA. This site is unofficial and independent of the FDA.