KCR · Class I · 21 CFR 872.3220

FDA Product Code KCR: Facebow

Leading manufacturers include Almore Intl., Inc..

1

Total

1

Cleared

48d

Avg days

1983

Since

FDA 510(k) Cleared Facebow Devices (Product Code KCR)

1 devices

1–1 of 1

Cleared Apr 28, 1983

FACEBOW FOR BALANCE ARTICULATOR

Almore Intl., Inc.

About Product Code KCR - Regulatory Context

Related FDA 510(k) Regulatory Insights

Data Source

FDA 510(k) public files . 175,972 total devices indexed.

Latest clearance: Apr 28, 1983

Product Code Info

Code	KCR
Device class	Class I
CFR	21 CFR 872.3220
Panel	Dental

Verify on FDA.gov

View KCR classification on FDA.gov →