The following data is part of a premarket notification filed by Bellingham Medical, Inc. with the FDA for Dermaseal.
Device ID | K960847 |
510k Number | K960847 |
Device Name: | DERMASEAL |
Classification | Dressing, Wound And Burn, Occlusive |
Applicant | BELLINGHAM MEDICAL, INC. 2401 PILOT KNOB RD., SUITE 118 Mendota Heights, MN 55120 |
Contact | Julia Lord |
Correspondent | Julia Lord BELLINGHAM MEDICAL, INC. 2401 PILOT KNOB RD., SUITE 118 Mendota Heights, MN 55120 |
Product Code | MGP |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-02-21 |
Decision Date | 1996-04-04 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DERMASEAL 88795696 not registered Live/Pending |
MEMDEM, Inc 2020-02-13 |
DERMASEAL 86113948 not registered Dead/Abandoned |
Adhezion Biomedical, LLC 2013-11-08 |
DERMASEAL 77510281 not registered Dead/Abandoned |
Adhezion Biomedical LLC 2008-06-27 |
DERMASEAL 75266893 2152292 Live/Registered |
Hydromer, Inc. 1997-03-31 |
DERMASEAL 75113280 2478260 Dead/Cancelled |
EVEREADY BATTERY COMPANY, INC. 1996-06-03 |
DERMASEAL 74623775 not registered Dead/Abandoned |
Derme, Inc. 1995-01-20 |