The following data is part of a premarket notification filed by Hill-rom, Inc. with the FDA for General Procedural Stretchers (p880- P886).
| Device ID | K922809 |
| 510k Number | K922809 |
| Device Name: | GENERAL PROCEDURAL STRETCHERS (P880- P886) |
| Classification | Stretcher, Wheeled |
| Applicant | HILL-ROM, INC. HIGHWAY 46 Batesville, TN |
| Contact | Ford Wilder |
| Correspondent | Ford Wilder HILL-ROM, INC. HIGHWAY 46 Batesville, TN |
| Product Code | FPO |
| CFR Regulation Number | 880.6910 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-06-10 |
| Decision Date | 1993-03-31 |