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SFQClass II

Electrosurgical, Cutting & Coagulation & Accessories, For Cardiac Electrophysiology Device Implantation And Revision

21 CFR 878.4400 / General, Plastic Surgery
FDA source (opens on fda.gov)

SFQ is the FDA product code for Electrosurgical, Cutting & Coagulation & Accessories, For Cardiac Electrophysiology Device Implantation And Revision, a class II device type, regulated under 21 CFR 878.4400. FDA's definition for this code reads: "Surgical device used to dissect cardiac tissue for the implantation and revision of cardiac electrophysiology leads". As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
SFQ
Device name
Electrosurgical, Cutting & Coagulation & Accessories, For Cardiac Electrophysiology Device Implantation And Revision
FDA definition
Surgical device used to dissect cardiac tissue for the implantation and revision of cardiac electrophysiology leads
Regulation
21 CFR 878.4400
Device class
Class II
Review panel
General, Plastic Surgery
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
0

Companies listing this code with FDA

Companies whose registered establishments list this code