The following data is part of a premarket notification filed by L.d. Technology, Llc with the FDA for Electro Interstitial Scan.
Device ID | K102166 |
510k Number | K102166 |
Device Name: | ELECTRO INTERSTITIAL SCAN |
Classification | Device, Galvanic Skin Response Measurement |
Applicant | L.D. TECHNOLOGY, LLC 11459 NW 34 STREET Miami, FL 33178 |
Contact | Richard Clement |
Correspondent | Richard Clement L.D. TECHNOLOGY, LLC 11459 NW 34 STREET Miami, FL 33178 |
Product Code | GZO |
CFR Regulation Number | 882.1540 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-08-02 |
Decision Date | 2010-12-10 |
Summary: | summary |