GARAVENTA X3 INCLINED PLATFORM LIFT
FDA 510(k) clearance K122206 · decided 2013-03-21
Clearance details
- K-number
- K122206
- Device name
- GARAVENTA X3 INCLINED PLATFORM LIFT
- Applicant
- Garaventa (Canada) Ltd [Dba Garaventa Lift]
- Decision
- Substantially Equivalent
- Date received
- 2012-07-25
- Decision date
- 2013-03-21
- Days to decision
- 239 days
- Clearance type
- Special
- Product code
- PCE
- Device class
- 2
- Regulation number
- 890.3930
- Medical specialty
- Physical Medicine
- Advisory committee
- Physical Medicine
- Location
- Roswell, GA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.