INTIMOL
Lubricant, Personal
DLC LABORATORIES, INC.
The following data is part of a premarket notification filed by Dlc Laboratories, Inc. with the FDA for Intimol.
Pre-market Notification Details
| Device ID | K061466 |
| 510k Number | K061466 |
| Device Name: | INTIMOL |
| Classification | Lubricant, Personal |
| Applicant | DLC LABORATORIES, INC. 7008 MARCELLE STREET Paramount, CA 90723 |
| Contact | Juan Manzur |
| Correspondent | Juan Manzur DLC LABORATORIES, INC. 7008 MARCELLE STREET Paramount, CA 90723 |
| Product Code | NUC |
| CFR Regulation Number | 884.5300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-05-26 |
| Decision Date | 2006-12-04 |
| Summary: | summary |
Trademark Results [INTIMOL]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 INTIMOL 78644858 3331093 Dead/Cancelled |
DLC Laboratories, Inc. 2005-06-07 |
 INTIMOL 76301132 not registered Dead/Abandoned |
Soft Gel Technologies, Inc. 2001-08-20 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.