The following data is part of a premarket notification filed by Plastic Applications, Inc. with the FDA for Tassaway.
| Device ID | K803250 |
| 510k Number | K803250 |
| Device Name: | TASSAWAY |
| Classification | Cup, Menstrual |
| Applicant | PLASTIC APPLICATIONS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HHE |
| CFR Regulation Number | 884.5400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-12-23 |
| Decision Date | 1981-02-12 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() TASSAWAY 74476910 not registered Dead/Abandoned |
Personal Care-Tech, Inc. 1994-01-06 |
![]() TASSAWAY 73361803 not registered Dead/Abandoned |
PLASTIC APPLICATIONS, INC. 1982-04-27 |
![]() TASSAWAY 72343015 0902277 Dead/Expired |
TASSETTE, INC. 1969-11-07 |