The following data is part of a premarket notification filed by Ken Kemmerer with the FDA for A.c. Power Patient Lift.
| Device ID | K935351 |
| 510k Number | K935351 |
| Device Name: | A.C. POWER PATIENT LIFT |
| Classification | Lift, Patient, Ac-powered |
| Applicant | KEN KEMMERER 788 KEATING ST. Wilkes Barre Twp, PA 18702 |
| Contact | Ken Kemmerer |
| Correspondent | Ken Kemmerer KEN KEMMERER 788 KEATING ST. Wilkes Barre Twp, PA 18702 |
| Product Code | FNG |
| CFR Regulation Number | 880.5500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-11-05 |
| Decision Date | 1994-02-28 |