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 ID | K152216 |
| 510k Number | K152216 |
| Device Name: | SudoC |
| Classification | Device, Galvanic Skin Response Measurement |
| Applicant | LD TECHNOLOGY LLC 100N. BIscayne Blvd, Suite 500 Miami, FL 33132 |
| Contact | Albert Maarek |
| Correspondent | Albert Maarek LD TECHNOLOGY LLC 100N. BIscayne Blvd, Suite 500 Miami, FL 33132 |
| Product Code | GZO |
| CFR Regulation Number | 882.1540 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-08-07 |
| Decision Date | 2015-09-24 |
| Summary: | summary |
NIH GUDID Devices
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| B322A0011 | K152216 | 000 |
Trademark Results [SudoC]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SUDOC 88916977 not registered Live/Pending |
SUDOC, LLC 2020-05-14 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.