MEDI BUTLER— 510(k) K051324
Substantially EquivalentMedi USA, LP
FDA 510(k) clearance K051324 for MEDI BUTLER, Substantially Equivalent on 2005-12-05. Applicant: Medi USA, LP. Device class: 2.
Clearance details
- Applicant
- Medi USA, LP
- Product code
- Code DWL
- Device class
- Class 2
- Regulation
- 21 CFR 880.5780
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
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