Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K130405Substantially Equivalent

Rusch Easycric Emergency Cricothyrotomy Set

Teleflex Medical, Durham NC / Traditional, Substantially Equivalent

K130405 is the FDA 510(k) clearance record for RUSCH EASYCRIC EMERGENCY CRICOTHYROTOMY SET, a class II device, cleared for Teleflex Medical on under FDA product code BWC (Needle, Emergency Airway). FDA records list 80 510(k) clearances for Teleflex Medical, from to . As of , FDA records show no recalls naming K130405.

Clearance record

Decision date
Received
(260 days to decision)
Product code
BWC Needle, Emergency Airway
Regulation
21 CFR 868.5090
Device class
Class II
Review panel
Anesthesiology
Applicant
Teleflex Medical 2917 Weck Dr., Durham NC
510(k) summary
Summary PDF
Third party review
No

Clearances, product code BWC

Trailing 12 months

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

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