The following data is part of a premarket notification filed by Dlc Laboratories, Inc. with the FDA for Intimol.
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 |
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 |