DeviceClearance

Product code CCW— Anesthesiology

LARYNGOSCOPE

Classification name
Laryngoscope, Rigid
Device class
Class 1
Regulation
21 CFR 868.5540
Advisory panel
Anesthesiology
Total cleared
64
First cleared
Most recent

Market context for product code CCW

FDA has cleared 64 devices under product code CCW between 1980 and 2019, filed by 52 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

Clearances per year

last 15 years

Top applicants under product code CCW

Adverse events under product code CCW

product code CCW
Death
31
Injury
136
Malfunction
3,703
Other
1
Total
3,871

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 CCW

Data sourced from openFDA. This site is unofficial and independent of the FDA.