The following data is part of a premarket notification filed by Ld Technology Llc with the FDA for Sudoc.
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 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
B322A0011 | K152216 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SUDOC 88916977 not registered Live/Pending |
SUDOC, LLC 2020-05-14 |