VAKUTAGE
Curette, Suction, Endometrial (and Accessories)
WESTON, COPCO, INC.
The following data is part of a premarket notification filed by Weston, Copco, Inc. with the FDA for Vakutage.
Pre-market Notification Details
| Device ID | K823080 |
| 510k Number | K823080 |
| Device Name: | VAKUTAGE |
| Classification | Curette, Suction, Endometrial (and Accessories) |
| Applicant | WESTON, COPCO, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HHK |
| CFR Regulation Number | 884.1175 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-10-19 |
| Decision Date | 1982-11-24 |
Trademark Results [VAKUTAGE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 VAKUTAGE 72454547 0992618 Dead/Expired |
WARNER-LAMBERT COMPANY 1973-04-13 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.