LH-75T PHOTOTHERAPY SYSTEM

Light, Ultraviolet, Dermatological

LERNER MEDICAL DEVICES, INC.

The following data is part of a premarket notification filed by Lerner Medical Devices, Inc. with the FDA for Lh-75t Phototherapy System.

Pre-market Notification Details

Device IDK090097
510k NumberK090097
Device Name:LH-75T PHOTOTHERAPY SYSTEM
ClassificationLight, Ultraviolet, Dermatological
Applicant LERNER MEDICAL DEVICES, INC. 1545 SAWTELLE BLVD., SUITE 36 Los Angeles,  CA  90025
ContactZafirios Gourgouliatos
CorrespondentZafirios Gourgouliatos
LERNER MEDICAL DEVICES, INC. 1545 SAWTELLE BLVD., SUITE 36 Los Angeles,  CA  90025
Product CodeFTC  
CFR Regulation Number878.4630 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2009-01-15
Decision Date2009-02-26
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
B280A0005400 K090097 000

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