SOLOLIFT - PATIENT TRANSFER STRETCHER

Device, Transfer, Patient, Manual

ADEL MEDICAL LTD.

The following data is part of a premarket notification filed by Adel Medical Ltd. with the FDA for Sololift - Patient Transfer Stretcher.

Pre-market Notification Details

Device IDK871475
510k NumberK871475
Device Name:SOLOLIFT - PATIENT TRANSFER STRETCHER
ClassificationDevice, Transfer, Patient, Manual
Applicant ADEL MEDICAL LTD. 16700 S.E. 120TH AVE. P.O. BOX 542 Clackamas,  OR  97015
ContactDavid R Cole
CorrespondentDavid R Cole
ADEL MEDICAL LTD. 16700 S.E. 120TH AVE. P.O. BOX 542 Clackamas,  OR  97015
Product CodeFMR  
CFR Regulation Number880.6785 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1987-04-14
Decision Date1987-05-11

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