GENESIS TOUCH SYSTEM

Transmitters And Receivers, Physiological Signal, Radiofrequency

HONEYWELL HOMMED

The following data is part of a premarket notification filed by Honeywell Hommed with the FDA for Genesis Touch System.

Pre-market Notification Details

Device IDK141792
510k NumberK141792
Device Name:GENESIS TOUCH SYSTEM
ClassificationTransmitters And Receivers, Physiological Signal, Radiofrequency
Applicant HONEYWELL HOMMED 3400 INTERTECH DRIVE Brookfield,  WI  53045
ContactClaudia Jackson
CorrespondentClaudia Jackson
HONEYWELL HOMMED 3400 INTERTECH DRIVE Brookfield,  WI  53045
Product CodeDRG  
CFR Regulation Number870.2910 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2014-07-02
Decision Date2014-11-25
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00817644020147 K141792 000
00817644020130 K141792 000
00817644020154 K141792 000

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