The following data is part of a premarket notification filed by J.b. Murray Enterprises, Inc. with the FDA for Murray Chair Lift.
| Device ID | K854120 |
| 510k Number | K854120 |
| Device Name: | MURRAY CHAIR LIFT |
| Classification | Lift, Patient, Ac-powered |
| Applicant | J.B. MURRAY ENTERPRISES, INC. 301 E. KALAMAZOO ST. P.O. BOX 145 Bloomingdale, MI 49026 |
| Contact | Charles Wilson |
| Correspondent | Charles Wilson J.B. MURRAY ENTERPRISES, INC. 301 E. KALAMAZOO ST. P.O. BOX 145 Bloomingdale, MI 49026 |
| Product Code | FNG |
| CFR Regulation Number | 880.5500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-10-09 |
| Decision Date | 1985-11-01 |