IDF — Acid, Fuchsin Class I

FDA Device Classification

FDA product code IDF covers "Acid, Fuchsin", a Class I medical device regulated under 21 CFR 864.1850. Submissions are reviewed by the Hematology panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

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

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K871545sigma diagnosticsNEW FUCHSIN SOLUTIONApril 29, 1987