The following data is part of a premarket notification filed by Personal Products Co. with the FDA for O.b. Tampon.
Device ID | K990536 |
510k Number | K990536 |
Device Name: | O.B. TAMPON |
Classification | Tampon, Menstrual, Unscented |
Applicant | PERSONAL PRODUCTS CO. 199 GRANDVIEW RD. Skillman, NJ 08558 |
Contact | Ralph Petrone |
Correspondent | Ralph Petrone PERSONAL PRODUCTS CO. 199 GRANDVIEW RD. Skillman, NJ 08558 |
Product Code | HEB |
CFR Regulation Number | 884.5470 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-02-19 |
Decision Date | 1999-08-31 |
Summary: | summary |