510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K761258Substantially Equivalent

Dover Low Pressure Tracheal Tube

Will Ross Co., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K761258 is the FDA 510(k) clearance record for DOVER LOW PRESSURE TRACHEAL TUBE, a class II device, cleared for Will Ross Co. on under FDA product code BTO (Tube, Tracheostomy (W/Wo Connector)). FDA records list 14 510(k) clearances for Will Ross Co., from to . As of , FDA records show no recalls naming K761258.

Clearance record

Decision date
Received
(8 days to decision)
Product code
BTO Tube, Tracheostomy (W/Wo Connector)
Regulation
21 CFR 868.5800
Device class
Class II
Review panel
Anesthesiology
Applicant
Will Ross Co. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code BTO

Trailing 12 months
1 clearance under product code BTO in the twelve months to October 2026, September 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code BTO, 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 20261
October 20260