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 |