SudoC

Device, Galvanic Skin Response Measurement

LD TECHNOLOGY LLC

The following data is part of a premarket notification filed by Ld Technology Llc with the FDA for Sudoc.

Pre-market Notification Details

Device IDK152216
510k NumberK152216
Device Name:SudoC
ClassificationDevice, Galvanic Skin Response Measurement
Applicant LD TECHNOLOGY LLC 100N. BIscayne Blvd, Suite 500 Miami,  FL  33132
ContactAlbert Maarek
CorrespondentAlbert Maarek
LD TECHNOLOGY LLC 100N. BIscayne Blvd, Suite 500 Miami,  FL  33132
Product CodeGZO  
CFR Regulation Number882.1540 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2015-08-07
Decision Date2015-09-24
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
B322A0011 K152216 000

Trademark Results [SudoC]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SUDOC
SUDOC
88916977 not registered Live/Pending
SUDOC, LLC
2020-05-14

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