The following data is part of a premarket notification filed by Non-friction Products Inc. with the FDA for Fuckwater.
| Device ID | K171730 |
| 510k Number | K171730 |
| Device Name: | FuckWater |
| Classification | Lubricant, Personal |
| Applicant | Non-Friction Products Inc. 551 Church Street Toronto, CA M4y 2e2 |
| Contact | Marc Barrette |
| Correspondent | James W. Monroe Monroe Medical Device Consulting, LLC 319 Shilling Dr Somerset, NJ 08873 |
| Product Code | NUC |
| CFR Regulation Number | 884.5300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-06-12 |
| Decision Date | 2017-09-07 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10796494002527 | K171730 | 000 |
| 10796494002510 | K171730 | 000 |
| 10796494002503 | K171730 | 000 |
| 10796494002466 | K171730 | 000 |
| 10796494002398 | K171730 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() FUCKWATER 87727118 not registered Live/Pending |
Non-Friction Products Inc. 2017-12-19 |