KCG · Class I · 21 CFR 874.4420

FDA Product Code KCG: Dilator, Tracheal

Leading manufacturers include Kelleher Corp..

1

Total

1

Cleared

35d

Avg days

1982

Since

FDA 510(k) Cleared Dilator, Tracheal Devices (Product Code KCG)

1 devices

1–1 of 1

Cleared Sep 02, 1982

TRACHEAL DILATORS

Ear, Nose, Throat · 35d

About Product Code KCG - Regulatory Context

Related FDA 510(k) Regulatory Insights

Data Source

FDA 510(k) public files . 175,730 total devices indexed.

Latest clearance: Sep 02, 1982

Product Code Info

Code	KCG
Device class	Class I
CFR	21 CFR 874.4420
Panel	Ear, Nose, Throat

Verify on FDA.gov

View KCG classification on FDA.gov →