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 |