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 |