SGFHumanitarian device exemption

Dural Arteriovenous Fistula Liquid Embolic

Unknown

SGF is the FDA product code for Dural Arteriovenous Fistula Liquid Embolic. FDA's definition for this code reads: "Indicated for use in the treatment of intracranial dural arteriovenous fistulas". As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: SGF
Device name: Dural Arteriovenous Fistula Liquid Embolic
FDA definition: Indicated for use in the treatment of intracranial dural arteriovenous fistulas.
Device class: Humanitarian device exemption
Review panel: Unknown
Submission type: FDA code 6
Implant: Yes
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

Terumo Cardiovascular Systems Corporation

Recent clearances

Product code SGF

FDA records hold no clearances under product code SGF.

Recent recalls

Product code SGF

FDA records show no recalls under product code SGF.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)