QUICK UP
Resin, Denture, Relining, Repairing, Rebasing
VOCO GMBH
The following data is part of a premarket notification filed by Voco Gmbh with the FDA for Quick Up.
Pre-market Notification Details
| 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 |
NIH GUDID Devices
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| E22116281 | K110440 | 000 |
| E22116271 | K110440 | 000 |
| E22116261 | K110440 | 000 |
Trademark Results [QUICK UP]
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 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.