The following data is part of a premarket notification filed by Procter & Gamble Mfg. Co. with the FDA for Scented Always Pantiliners.
Device ID | K853000 |
510k Number | K853000 |
Device Name: | SCENTED ALWAYS PANTILINERS |
Classification | Pad, Menstrual, Scented |
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 | HHL |
CFR Regulation Number | 884.5425 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-07-15 |
Decision Date | 1985-09-06 |