510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K913876Substantially Equivalent

Endotracheal Suctiontube

Willowtech, Fort Worth TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K913876 is the FDA 510(k) clearance record for ENDOTRACHEAL SUCTIONTUBE, a class II device, cleared for Willowtech on under FDA product code JOL (Catheter And Tip, Suction). FDA records list one 510(k) clearance for Willowtech. As of , FDA records show no recalls naming K913876.

Clearance record

Decision date
Received
(190 days to decision)
Product code
JOL Catheter And Tip, Suction
Regulation
21 CFR 880.6740
Device class
Class II
Review panel
General Hospital
Applicant
Willowtech P.O. Box 185789, Fort Worth TX
510(k) summary
Statement
Third party review
No

Clearances, product code JOL

Trailing 12 months

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

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