510(k) K061726
K061726 is an FDA 510(k) premarket notification submitted by Lifestand for the device "LSC, MODEL 3". The FDA issued a decision of Substantially Equivalent on December 4, 2006. The device falls under product code IPL (Wheelchair, Standup), a Class II device regulated under 21 CFR 890.3900. Lifestand has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 4, 2006
- Date Received
- June 19, 2006
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Wheelchair, Standup
- Device Class
- Class II
- Regulation Number
- 890.3900
- Review Panel
- PM
- Submission Type