DRI SLEEPER

Alarm, Conditioned Response Enuresis

LABORIE MEDICAL TECHNOLOGIES, LTD.

The following data is part of a premarket notification filed by Laborie Medical Technologies, Ltd. with the FDA for Dri Sleeper.

Pre-market Notification Details

Device IDK934369
510k NumberK934369
Device Name:DRI SLEEPER
ClassificationAlarm, Conditioned Response Enuresis
Applicant LABORIE MEDICAL TECHNOLOGIES, LTD. 6415 NORTHWEST DR. UNIT 11 Mississauga (ontario),  CA L4v 1x1
ContactFred Buffa
CorrespondentFred Buffa
LABORIE MEDICAL TECHNOLOGIES, LTD. 6415 NORTHWEST DR. UNIT 11 Mississauga (ontario),  CA L4v 1x1
Product CodeKPN  
CFR Regulation Number876.2040 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1993-09-07
Decision Date1993-11-24

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