The following data is part of a premarket notification filed by Dalton Instrument Corp. with the FDA for Dalton Lift Chair.
| Device ID | K131909 |
| 510k Number | K131909 |
| Device Name: | DALTON LIFT CHAIR |
| Classification | Chair, Positioning, Electric |
| Applicant | DALTON INSTRUMENT CORP. 16300 Addison Rd Ste 120 Addison, TX 75001 |
| Contact | Mei Lein |
| Correspondent | Mei Lein DALTON INSTRUMENT CORP. 16300 Addison Rd Ste 120 Addison, TX 75001 |
| Product Code | INO |
| CFR Regulation Number | 890.3110 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-06-26 |
| Decision Date | 2014-02-24 |
| Summary: | summary |