The following data is part of a premarket notification filed by Probed Medical Technologies, Inc. with the FDA for The Freedom Bed.
| Device ID | K954671 |
| 510k Number | K954671 |
| Device Name: | THE FREEDOM BED |
| Classification | Bed, Patient Rotation, Powered |
| Applicant | PROBED MEDICAL TECHNOLOGIES, INC. 44325 YALE RD. WEST Chilliwack, B.c., CA V2r 4h2 |
| Contact | Steve Plummer |
| Correspondent | Steve Plummer PROBED MEDICAL TECHNOLOGIES, INC. 44325 YALE RD. WEST Chilliwack, B.c., CA V2r 4h2 |
| Product Code | IKZ |
| CFR Regulation Number | 890.5225 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-10-10 |
| Decision Date | 1996-04-01 |
| Summary: | summary |