510(k) K011983

Device
INSIGHT GENESIS
Applicant
Fasstech
510(k) number
K011983
Product code
HCC
Decision
Substantially Equivalent (SESE)
Decision date
2001-08-30
Date received
2001-06-26
Regulation
882.5050
Classification name
Device, Biofeedback
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
LEE BRODY
Address
155 Middlesex Tpke. Burlington MA US 01803 01803

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code HCC#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K233580A Breathing System (ABS)Deepwell Dtx, Inc.2024-08-01
K222101PrismGraymatters Health , Ltd.2023-03-17
K180173FreespiraPalo Alto Health Sciences, Inc.2018-08-23
K163448GrindCare SystemSunstar Suisse S.A.2017-09-01
K151050Pacifier Activated Lullaby (PALĀ®)Power Medical Devices, LLC2015-12-22
K143507NFANT Feeding SolutionNfant Labs, LLC2015-09-09
K131586CANARY BREATHING SYSTEMPalo Alto Health Sciences, Inc.2013-12-10
K122879EEGER4 MODEL 4.3Eeg Software, LLC2013-02-06
K111687EMG SYSTEMMyotronics-Noromed, Inc.2011-09-29
K092675GRINDCAREMedotech A/S2010-03-03
K073557EEG NEUROAMP, MODEL CS10137Corscience GmbH & Co. KG2008-02-28
K071866NTRAINER SYSTEMKcbiomedix, Inc.2008-02-01
K071661ALPHAONE BIOFEEDBACK SYSTEMTelediagnostic Systems, Inc.2007-09-05
K041244POLYGRAM NET BIOFEEDBACK APPLICATIONMedtronic Vascular2004-08-12
K020399RESPERATE; MODEL RR-150Intercure , Ltd.2002-07-02