The following data is part of a premarket notification filed by Edson Corp. with the FDA for Wet Sense.
| Device ID | K935915 |
| 510k Number | K935915 |
| Device Name: | WET SENSE |
| Classification | Alarm, Conditioned Response Enuresis |
| Applicant | EDSON CORP. 24015 CREEK WOOD DR. Spring, TX 77389 |
| Product Code | KPN |
| CFR Regulation Number | 876.2040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-12-09 |
| Decision Date | 1994-05-13 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() WET SENSE 78622056 not registered Dead/Abandoned |
Tyco Healthcare Retail Services AG 2005-05-04 |