The following data is part of a premarket notification filed by Summit Lifts, Inc. with the FDA for Summit Stairway Lift.
| Device ID | K032880 |
| 510k Number | K032880 |
| Device Name: | SUMMIT STAIRWAY LIFT |
| Classification | Transport, Patient, Powered |
| Applicant | SUMMIT LIFTS, INC. 7300 W. 110TH STREET SUITE 260 Overland Park, KS 66210 |
| Contact | Kent Perry |
| Correspondent | Kent Perry SUMMIT LIFTS, INC. 7300 W. 110TH STREET SUITE 260 Overland Park, KS 66210 |
| Product Code | ILK |
| CFR Regulation Number | 890.5150 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-09-15 |
| Decision Date | 2003-11-10 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00817650022715 | K032880 | 000 |
| 00817650022708 | K032880 | 000 |
| 00817650022661 | K032880 | 000 |
| 00817650022654 | K032880 | 000 |