510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K935842Substantially Equivalent

Rusch Lasertubus/rusch Laser Resistant Cuffed with Murphy Eye

Rusch, Inc., Duluth GA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K935842 is the FDA 510(k) clearance record for RUSCH LASERTUBUS/RUSCH LASER RESISTANT CUFFED WITH MURPHY EYE, a class II device, cleared for Rusch, Inc. on under FDA product code BTR (Tube, Tracheal (W/Wo Connector)). FDA records list 6 510(k) clearances for Rusch, Inc., from to . As of , FDA records show 7 recalls naming K935842.

Clearance record

Decision date
Received
(532 days to decision)
Product code
BTR Tube, Tracheal (W/Wo Connector)
Regulation
21 CFR 868.5730
Device class
Class II
Review panel
Anesthesiology
Applicant
Rusch, Inc. 2450 Meadowbrook Pkwy., Duluth GA
510(k) summary
Statement
Third party review
No

Clearances, product code BTR

Trailing 12 months
2 clearances under product code BTR in the twelve months to October 2026, June 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code BTR, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20261
October 20260