EarlySense Bed Sensing Unit

Monitor, Breathing Frequency

EarlySense Ltd.

The following data is part of a premarket notification filed by Earlysense Ltd. with the FDA for Earlysense Bed Sensing Unit.

Pre-market Notification Details

Device IDK171836
510k NumberK171836
Device Name:EarlySense Bed Sensing Unit
ClassificationMonitor, Breathing Frequency
Applicant EarlySense Ltd. 7 Derech Zeev Jabotinsky Ramat Gan,  IL 5252007
ContactDalia Argaman
CorrespondentDalia Argaman
EarlySense Ltd. 7 Derech Zeev Jabotinsky Ramat Gan,  IL 5252007
Product CodeBZQ  
CFR Regulation Number868.2375 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2017-06-20
Decision Date2018-01-04
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
17290016169246 K171836 000

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