MSI 3003 SERIES BED

Bed, Manual

MED SERVICE, INC.

The following data is part of a premarket notification filed by Med Service, Inc. with the FDA for Msi 3003 Series Bed.

Pre-market Notification Details

Device IDK881964
510k NumberK881964
Device Name:MSI 3003 SERIES BED
ClassificationBed, Manual
Applicant MED SERVICE, INC. P.O. BOX 1296 HWY. 6 WEST Batesville,  MS  38606
ContactBruce Baggett
CorrespondentBruce Baggett
MED SERVICE, INC. P.O. BOX 1296 HWY. 6 WEST Batesville,  MS  38606
Product CodeFNJ  
CFR Regulation Number880.5120 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1988-05-10
Decision Date1988-06-28

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.