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Applicator (Laryngo-Tracheal), Topical Anesthesia

FDA product code CCT · Class 2 · Anesthesiology

37
Registered devices
24
Adverse events
6
Recalls
10
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2018-03-19Teleflex Medical Europe LtdTeleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label.
2017-07-05Teleflex MedicalTeleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label.
2016-10-27Teleflex MedicalProduct Defect; These products may produce a straight stream instead of a fully atomized plume of medication.
2009-03-05Sharn, Inc.Sharn Anesthesia Inc., Tampa, FL received reports of leaking containers following use of their Sharn Anesthesia Microblast nasal and pediatric laryngeal atomize
2009-03-05Sharn, Inc.Sharn Anesthesia Inc., Tampa, FL received reports of leaking containers following use of their Sharn Anesthesia Microblast nasal and pediatric laryngeal atomize
2009-03-05Sharn, Inc.Sharn Anesthesia Inc., Tampa, FL received reports of leaking containers following use of their Sharn Anesthesia Microblast nasal and pediatric laryngeal atomize

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.