Product code CCT— Anesthesiology
ANESTHESIA KIT
- Classification name
- Applicator (Laryngo-Tracheal), Topical Anesthesia
- Device class
- Class 2
- Regulation
- 21 CFR 868.5170
- Advisory panel
- Anesthesiology
- Total cleared
- 10
- First cleared
- Most recent
Market context for product code CCT
FDA has cleared devices under product code CCT between 1976 and 2024, filed by 9 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
- 2024
- 2018
- 2016
- 2011
- 2007
- 2000
- 1990
- 1981
- 1976
Top applicants under product code CCT
Adverse events under product code CCT
product code CCT- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recent clearances under product code CCT
- K240114 — UltraEzAir® (UEA1A)
- K172956 — Medicant Mucosal Atomizer
- K153470 — MADgic Laryngo-Tracheal Mucosal Atomization Device
- K093584 — EZ-MISTER
- K070596 — TOPICAL APPLICATOR
- K002255 — LARYNGO-TRACHEAL MUCOSAL ATOMIZATION DEVICE (MADGIC)
- K894755 — ASTRA DISPOSABLE SPRAY CANNULA
- K810059 — ENDO-MED TUBE FOR ENDOTRACHEAL MED
- K760759 — ANESTHESIA KIT
- K760877 — MONOJECT LARYNGOTRACHEAL ANESTHESIA KIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.