KBO · Class I · 21 CFR 874.4420

FDA Product Code KBO: Guillotine, Tonsil

Leading manufacturers include Kelleher Corp..

1

Total

1

Cleared

32d

Avg days

1982

Since

FDA 510(k) Cleared Guillotine, Tonsil Devices (Product Code KBO)

1 devices

1–1 of 1

Cleared Aug 30, 1982

MYLE'S GUILLOTINE

Ear, Nose, Throat · 32d

About Product Code KBO - Regulatory Context

Related FDA 510(k) Regulatory Insights

Data Source

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

Latest clearance: Aug 30, 1982

Product Code Info

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

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