510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K903856Substantially Equivalent

Wet-No-More Monitor

Travis Industries, Inc., Coos Bay OR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K903856 is the FDA 510(k) clearance record for WET-NO-MORE MONITOR, a class II device, cleared for Travis Industries, Inc. on under FDA product code KPN (Alarm, Conditioned Response Enuresis). FDA records list 3 510(k) clearances for Travis Industries, Inc., from to . As of , FDA records show no recalls naming K903856.

Clearance record

Decision date
Received
(50 days to decision)
Product code
KPN Alarm, Conditioned Response Enuresis
Regulation
21 CFR 876.2040
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Travis Industries, Inc. 100 Main-Sumner, Coos Bay OR
Third party review
No

Clearances, product code KPN

Trailing 12 months

FDA records hold no clearances under product code KPN in the trailing twelve months.

FDA records show no clearances under product code KPN in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KPN, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260