Device
Atlas
510(k)
Recalls
Companies
Specialties
Home
›
General, Plastic Surgery
›
KAG – Holder, Speculum, Ent
Holder, Speculum, Ent
FDA product code
KAG
· Class I (low risk) · 21 CFR 878.1800 ·
General, Plastic Surgery
2
510(k) clearances
0
PMA approvals
0
recalls
Manufacturers
Cardiac Pacemakers, Inc.
1
E K Ind., Inc.
1
510(k) clearances
510(k)
Device
Applicant
Decision
K842931
Drabkin Reagent
KAG · Traditional
E K Ind., Inc.
09/21/1984
SE
K822857
Cpi Printer
KAG · Traditional
Cardiac Pacemakers, Inc.
01/08/1983
SE