The following data is part of a premarket notification filed by Med Service, Inc. with the FDA for Msi 3003 Series Bed.
| Device ID | K881964 |
| 510k Number | K881964 |
| Device Name: | MSI 3003 SERIES BED |
| Classification | Bed, Manual |
| Applicant | MED SERVICE, INC. P.O. BOX 1296 HWY. 6 WEST Batesville, MS 38606 |
| Contact | Bruce Baggett |
| Correspondent | Bruce Baggett MED SERVICE, INC. P.O. BOX 1296 HWY. 6 WEST Batesville, MS 38606 |
| Product Code | FNJ |
| CFR Regulation Number | 880.5120 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-05-10 |
| Decision Date | 1988-06-28 |