DARClass II

Fibrinogen And Split Products, Rhodamine, Antigen, Antiserum, Control

21 CFR 864.7340 / Hematology

DAR is the FDA product code for Fibrinogen And Split Products, Rhodamine, Antigen, Antiserum, Control, a class II device type, regulated under 21 CFR 864.7340. As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: DAR
Device name: Fibrinogen And Split Products, Rhodamine, Antigen, Antiserum, Control
Regulation: 21 CFR 864.7340
Device class: Class II
Review panel: Hematology
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: Yes
Ingested clearances: 0
Ingested recalls: 0

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code DAR.

Recent clearances

Product code DAR

FDA records hold no clearances under product code DAR.

Recent recalls

Product code DAR

FDA records show no recalls under product code DAR.

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)