The following data is part of a premarket notification filed by Playtex, Inc. with the FDA for Playtex Process Machinery Change.
| Device ID | K811386 |
| 510k Number | K811386 |
| Device Name: | PLAYTEX PROCESS MACHINERY CHANGE |
| Classification | Tampon, Menstrual, Scented, Deodorized |
| Applicant | PLAYTEX, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HIL |
| CFR Regulation Number | 884.5460 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-05-18 |
| Decision Date | 1981-07-10 |