The following data is part of a premarket notification filed by Arylift, Inc. with the FDA for Patient Support System.
| Device ID | K940872 |
| 510k Number | K940872 |
| Device Name: | PATIENT SUPPORT SYSTEM |
| Classification | Lift, Patient, Ac-powered |
| Applicant | ARYLIFT, INC. 601 THIRTEENTH STREET, N.W. WASHINGTON, D.C., DC 20005 |
| Contact | TERRY G MAHN |
| Correspondent | TERRY G MAHN ARYLIFT, INC. 601 THIRTEENTH STREET, N.W. WASHINGTON, D.C., DC 20005 |
| Product Code | FNG |
| CFR Regulation Number | 880.5500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-02-25 |
| Decision Date | 1994-10-13 |