DeviceClearance

Product code CAP— Anesthesiology

AIRWAY PRESSURE MONITOR

Classification name
Monitor, Airway Pressure (Includes Gauge And/Or Alarm)
Device class
Class 2
Regulation
21 CFR 868.2600
Advisory panel
Anesthesiology
Total cleared
78
First cleared
Most recent

Market context for product code CAP

FDA has cleared 78 devices under product code CAP between 1978 and 2020, filed by 53 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

last 15 years

Top applicants under product code CAP

Recent clearances under product code CAP

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