KCY · Class I · 21 CFR 878.5910

FDA Product Code KCY: Tourniquet, Pneumatic

34
Total
34
Cleared
104d
Avg days
1978
Since
Stable submission activity - 0 submissions in the last 2 years

FDA 510(k) Cleared Tourniquet, Pneumatic Devices (Product Code KCY)

34 devices
1–24 of 34
No devices found for this product code.

About Product Code KCY - Regulatory Context

510(k) Submission Activity

34 total 510(k) submissions under product code KCY since 1978, with 34 receiving FDA clearance (average review time: 104 days).

Submission volume has remained relatively stable over the observed period, with 0 submissions in the last 24 months.