The following data is part of a premarket notification filed by Laivan Corp. with the FDA for Aquaderm.
Device ID | K885205 |
510k Number | K885205 |
Device Name: | AQUADERM |
Classification | Tape And Bandage, Adhesive |
Applicant | LAIVAN CORP. 49 FRONT ST. P.O. BOX 175 East Rockaway, NY 11518 |
Contact | Joel Martz |
Correspondent | Joel Martz LAIVAN CORP. 49 FRONT ST. P.O. BOX 175 East Rockaway, NY 11518 |
Product Code | KGX |
CFR Regulation Number | 880.5240 [🔎] |
Decision | Substantially Equivalent For Some Indications (SN) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-12-19 |
Decision Date | 1989-03-29 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
AQUADERM 88320615 not registered Live/Pending |
LAPKO Inc. 2019-02-28 |
AQUADERM 78777758 3180503 Dead/Cancelled |
Lanxess Deutschland GmbH 2005-12-21 |
AQUADERM 74663213 1986866 Dead/Cancelled |
Bayer Aktiengesellschaft 1995-04-19 |
AQUADERM 73757881 1578499 Dead/Cancelled |
BAKER CUMMINS LABORATORIES, INC. 1988-10-17 |
AQUADERM 73595621 not registered Dead/Abandoned |
LABORATOIRES ED. FROMONT 1986-04-28 |
AQUADERM 72183084 0779351 Dead/Expired |
MENLEY & JAMES LABORATORIES, LTD. 1963-12-16 |