The following data is part of a premarket notification filed by Med Service, Inc. with the FDA for Msi 2005 Series Bed.
Device ID | K881962 |
510k Number | K881962 |
Device Name: | MSI 2005 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 | 1988-06-03 |