The following data is part of a premarket notification filed by J. H. Emerson Co. with the FDA for Emerson Motion Bed 6-ms & 6-me.
| Device ID | K842604 |
| 510k Number | K842604 |
| Device Name: | EMERSON MOTION BED 6-MS & 6-ME |
| Classification | Bed, Patient Rotation, Powered |
| Applicant | J. H. EMERSON CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IKZ |
| CFR Regulation Number | 890.5225 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-07-05 |
| Decision Date | 1984-07-20 |