The following data is part of a premarket notification filed by J. T. Posey Co. with the FDA for Posey Bed.
| Device ID | K103817 |
| 510k Number | K103817 |
| Device Name: | POSEY BED |
| Classification | Patient Bed With Canopy/restraints |
| Applicant | J. T. POSEY CO. 5635 PECK RD. Arcadia, CA 91006 |
| Contact | Robert Kelleher |
| Correspondent | Robert Kelleher J. T. POSEY CO. 5635 PECK RD. Arcadia, CA 91006 |
| Product Code | OYS |
| CFR Regulation Number | 880.6760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-12-29 |
| Decision Date | 2011-04-22 |
| Summary: | summary |