Home / Device Classification / KFD

KFD — Aniline Blue Class I

FDA Device Classification

Classification Details

Product Code: KFD
Device Class: Class I
Regulation Number: 864.1850
Submission Type
Review Panel: PA
Medical Specialty: Hematology
Implant: No

Recent 510(k) Clearances

K-Number	Applicant	Device Name	Date
K894045	devetec	MODIFIED POLYCHROME IV STAIN	July 25, 1989