Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K946057Substantially Equivalent

Aqualarm Moisture Sensor Model P85000

Pegasus Research Corp., Costa Mesa CA / Traditional, Substantially Equivalent

K946057 is the FDA 510(k) clearance record for AQUALARM MOISTURE SENSOR MODEL P85000, a class I device, cleared for Pegasus Research Corp. on under FDA product code BYH (Drain, Tee (Water Trap)). FDA records list 12 510(k) clearances for Pegasus Research Corp., from to . As of , FDA records show no recalls naming K946057.

Clearance record

Decision date
Received
(144 days to decision)
Product code
BYH Drain, Tee (Water Trap)
Regulation
21 CFR 868.5995
Device class
Class I
Review panel
Anesthesiology
Applicant
Pegasus Research Corp. 775 W. 17th St. Suite D, Costa Mesa CA
510(k) summary
Summary
Third party review
No

Clearances, product code BYH

Trailing 12 months

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

FDA records show no clearances under product code BYH in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code BYH, 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