The following data is part of a premarket notification filed by Voco Gmbh with the FDA for Quick Up.
Device ID | K110440 |
510k Number | K110440 |
Device Name: | QUICK UP |
Classification | Resin, Denture, Relining, Repairing, Rebasing |
Applicant | VOCO GMBH ANTON-FLETTNER-STR. 1-3 Cuxhaven, DE 27472 |
Contact | Dr. T. Gerkensmeier |
Correspondent | Dr. T. Gerkensmeier VOCO GMBH ANTON-FLETTNER-STR. 1-3 Cuxhaven, DE 27472 |
Product Code | EBI |
CFR Regulation Number | 872.3760 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-02-15 |
Decision Date | 2011-05-04 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
E22116281 | K110440 | 000 |
E22116271 | K110440 | 000 |
E22116261 | K110440 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() QUICK UP 98231367 not registered Live/Pending |
Absorbent Specialty Products, LLC 2023-10-19 |
![]() QUICK UP 79101798 4116852 Live/Registered |
VOCO GmbH 2011-06-10 |
![]() QUICK UP 73512073 1344140 Live/Registered |
NATIONAL UNION ELECTRIC CORPORATION 1984-12-05 |