DCM 2.0— 510(k) K020971
Substantially EquivalentMds Nordion AB
FDA 510(k) clearance K020971 for DCM 2.0, Substantially Equivalent on 2002-06-06. Applicant: Mds Nordion AB. Device class: 2.
Clearance details
- Applicant
- Mds Nordion AB
- Product code
- Code MUJ
- Device class
- Class 2
- Regulation
- 21 CFR 892.5050
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Ottawa, CA
Recent devices under product code MUJ
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