MULTIDIAGNOST ELEVA
FDA 510(k) clearance K050151 · decided 2005-02-09
Clearance details
- K-number
- K050151
- Device name
- MULTIDIAGNOST ELEVA
- Applicant
- Philips Medical Systems North America, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2005-01-24
- Decision date
- 2005-02-09
- Days to decision
- 16 days
- Clearance type
- Traditional
- Product code
- KPR
- Device class
- 2
- Regulation number
- 892.1680
- Medical specialty
- Radiology
- Advisory committee
- Radiology
- Location
- Bothell, WA, US
- Third-party review
- Yes
- Expedited review
- No
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