The following data is part of a premarket notification filed by Tampax, Inc. with the FDA for Modified Untreated Tampax Tampons.
| Device ID | K780648 |
| 510k Number | K780648 |
| Device Name: | MODIFIED UNTREATED TAMPAX TAMPONS |
| Classification | Tampon, Menstrual, Unscented |
| Applicant | TAMPAX, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | HEB |
| CFR Regulation Number | 884.5470 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-04-17 |
| Decision Date | 1978-05-31 |