The following data is part of a premarket notification filed by Procter & Gamble Mfg. Co. with the FDA for Tampon, Rely Modified.
| Device ID | K780243 |
| 510k Number | K780243 |
| Device Name: | TAMPON, RELY MODIFIED |
| Classification | Tampon, Menstrual, Unscented |
| Applicant | PROCTER & GAMBLE MFG. CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HEB |
| CFR Regulation Number | 884.5470 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-02-13 |
| Decision Date | 1978-03-02 |