The following data is part of a premarket notification filed by Medical/surgical Specialties, Ltd. with the FDA for The Murray Mobilift(tm).
| Device ID | K895677 |
| 510k Number | K895677 |
| Device Name: | THE MURRAY MOBILIFT(TM) |
| Classification | Lift, Patient, Ac-powered |
| Applicant | MEDICAL/SURGICAL SPECIALTIES, LTD. 1611 W. CENTRE ST. Kalamazoo, MI 49002 |
| Contact | James L Phillips |
| Correspondent | James L Phillips MEDICAL/SURGICAL SPECIALTIES, LTD. 1611 W. CENTRE ST. Kalamazoo, MI 49002 |
| Product Code | FNG |
| CFR Regulation Number | 880.5500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-09-20 |
| Decision Date | 1990-10-26 |