ELECTRO INTERSTITIAL SCAN

Device, Galvanic Skin Response Measurement

L.D. TECHNOLOGY, LLC

The following data is part of a premarket notification filed by L.d. Technology, Llc with the FDA for Electro Interstitial Scan.

Pre-market Notification Details

Device IDK102166
510k NumberK102166
Device Name:ELECTRO INTERSTITIAL SCAN
ClassificationDevice, Galvanic Skin Response Measurement
Applicant L.D. TECHNOLOGY, LLC 11459 NW 34 STREET Miami,  FL  33178
ContactRichard Clement
CorrespondentRichard Clement
L.D. TECHNOLOGY, LLC 11459 NW 34 STREET Miami,  FL  33178
Product CodeGZO  
CFR Regulation Number882.1540 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2010-08-02
Decision Date2010-12-10
Summary:summary

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