The following data is part of a premarket notification filed by Procter & Gamble Co. with the FDA for Always Unscented Menstrual Pads.
Device ID | K884428 |
510k Number | K884428 |
Device Name: | ALWAYS UNSCENTED MENSTRUAL PADS |
Classification | Pad, Menstrual, Unscented |
Applicant | PROCTER & GAMBLE CO. LEGAL DIVISION 1 PROCTER & GAMBLE PLAZA Cincinnati, OH 45202 |
Contact | James T O'reilly |
Correspondent | James T O'reilly PROCTER & GAMBLE CO. LEGAL DIVISION 1 PROCTER & GAMBLE PLAZA Cincinnati, OH 45202 |
Product Code | HHD |
CFR Regulation Number | 884.5435 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-10-20 |
Decision Date | 1988-12-02 |