The following data is part of a premarket notification filed by Procter & Gamble Co. with the FDA for Tampax Tampons - (light,regular,super And Super Plus Absorbencies).
Device ID | K061486 |
510k Number | K061486 |
Device Name: | TAMPAX TAMPONS - (LIGHT,REGULAR,SUPER AND SUPER PLUS ABSORBENCIES) |
Classification | Tampon, Menstrual, Unscented |
Applicant | PROCTER & GAMBLE CO. 2001 PENNSYLVANIA AVE, STE 575 Washington, DC 20006 |
Contact | Philip J Phillips |
Correspondent | Philip J Phillips PROCTER & GAMBLE CO. 2001 PENNSYLVANIA AVE, STE 575 Washington, DC 20006 |
Product Code | HEB |
CFR Regulation Number | 884.5470 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-05-31 |
Decision Date | 2006-08-01 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00024291308461 | K061486 | 000 |