KAG · Class I · 21 CFR 878.1800

FDA Product Code KAG: Holder, Speculum, Ent

Leading manufacturers include Cardiac Pacemakers, Inc. and E K Ind., Inc..

2
Total
2
Cleared
81d
Avg days
1983
Since

FDA 510(k) Cleared Holder, Speculum, Ent Devices (Product Code KAG)

2 devices
1–2 of 2
Cleared Sep 21, 1984
DRABKIN REAGENT
K842931
E K Ind., Inc.
Hematology · 58d
Cleared Jan 08, 1983
CPI PRINTER
K822857
Cardiac Pacemakers, Inc.
General & Plastic Surgery · 103d

About Product Code KAG - Regulatory Context