Submission Details
| 510(k) Number | K091578 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | June 02, 2009 |
| Decision Date | December 02, 2009 |
| Days to Decision | 183 days |
| Submission Type | Special |
| Review Panel | Physical Medicine (PM) |
| Summary | Summary PDF |
K091578 is an FDA 510(k) clearance for the LIFT CHAIR, MODEL T3, a Chair, Positioning, Electric (Class II — Special Controls, product code INO), submitted by Pride Mobility Products Corp. (Exeter, US). The FDA issued a Cleared decision on December 2, 2009, 183 days after receiving the submission on June 2, 2009. This device falls under the Physical Medicine review panel. Regulated under 21 CFR 890.3110.
| 510(k) Number | K091578 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | June 02, 2009 |
| Decision Date | December 02, 2009 |
| Days to Decision | 183 days |
| Submission Type | Special |
| Review Panel | Physical Medicine (PM) |
| Summary | Summary PDF |
| Product Code | INO — Chair, Positioning, Electric |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 890.3110 |