Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K013856Substantially Equivalent

Pmh 1000 Heated Humidifier

Pegasus Research Corp., Santa Ana CA / Traditional, Substantially Equivalent

K013856 is the FDA 510(k) clearance record for PMH 1000 HEATED HUMIDIFIER, a class II device, cleared for Pegasus Research Corp. on under FDA product code BTT (Humidifier, Respiratory Gas, (Direct Patient Interface)). FDA records list 12 510(k) clearances for Pegasus Research Corp., from to . As of , FDA records show no recalls naming K013856.

Clearance record

Decision date
Received
(472 days to decision)
Product code
BTT Humidifier, Respiratory Gas, (Direct Patient Interface)
Regulation
21 CFR 868.5450
Device class
Class II
Review panel
Anesthesiology
Applicant
Pegasus Research Corp. 1714 S. Lyon St., Santa Ana CA
510(k) summary
Statement
Third party review
No

Clearances, product code BTT

Trailing 12 months
5 clearances under product code BTT in the twelve months to October 2026, January 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code BTT, trailing twelve months
MonthClearances
November 20250
December 20251
January 20262
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20261
September 20260
October 20260