The following data is part of a premarket notification filed by S & W Enterprises, Inc. with the FDA for S & W Sw52e W/power Back Lift.
| Device ID | K832768 |
| 510k Number | K832768 |
| Device Name: | S & W SW52E W/POWER BACK LIFT |
| Classification | Table, Examination, Medical, Powered |
| Applicant | S & W ENTERPRISES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | LGX |
| CFR Regulation Number | 878.4960 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-08-16 |
| Decision Date | 1983-09-20 |