The following data is part of a premarket notification filed by Hill-rom, Inc. with the FDA for Vacuum Power Body Fluid Suction Apparatus.
| Device ID | K926140 |
| 510k Number | K926140 |
| Device Name: | VACUUM POWER BODY FLUID SUCTION APPARATUS |
| Classification | Regulator, Vacuum |
| Applicant | HILL-ROM, INC. HIGHWAY 46 Batesville, TN |
| Contact | Ford Wilder |
| Correspondent | Ford Wilder HILL-ROM, INC. HIGHWAY 46 Batesville, TN |
| Product Code | KDP |
| CFR Regulation Number | 880.6740 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-12-07 |
| Decision Date | 1993-07-27 |