The following data is part of a premarket notification filed by Procter & Gamble Mfg. Co. with the FDA for Scented Menstrual Pad.
Device ID | K844602 |
510k Number | K844602 |
Device Name: | SCENTED MENSTRUAL PAD |
Classification | Pad, Menstrual, Unscented |
Applicant | PROCTER & GAMBLE MFG. CO. P.O. BOX 599 Cincinnati, OH 45201 |
Contact | James T O'reilly |
Correspondent | James T O'reilly PROCTER & GAMBLE MFG. CO. P.O. BOX 599 Cincinnati, OH 45201 |
Product Code | HHD |
CFR Regulation Number | 884.5435 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-11-27 |
Decision Date | 1985-01-16 |