ALWAYS DUETS
Pad, Menstrual, Unscented
PROCTER & GAMBLE CO.
The following data is part of a premarket notification filed by Procter & Gamble Co. with the FDA for Always Duets.
Pre-market Notification Details
| Device ID | K012629 |
| 510k Number | K012629 |
| Device Name: | ALWAYS DUETS |
| Classification | Pad, Menstrual, Unscented |
| Applicant | PROCTER & GAMBLE CO. 6110 CENTER HILL AVE. Cincinnati, OH 45224 |
| Contact | Mark M Anderson |
| Correspondent | Mark M Anderson PROCTER & GAMBLE CO. 6110 CENTER HILL AVE. Cincinnati, OH 45224 |
| Product Code | HHD |
| CFR Regulation Number | 884.5435 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-08-13 |
| Decision Date | 2001-10-05 |
| Summary: | summary |
Trademark Results [ALWAYS DUETS]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ALWAYS DUETS 78038746 not registered Dead/Abandoned |
Procter & Gamble Company, The 2000-12-11 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.