IGE — Solution, Formalin Ammonium Bromide Class I

FDA Device Classification

FDA product code IGE covers "Solution, Formalin Ammonium Bromide", a Class I medical device regulated under 21 CFR 864.4010. Submissions are reviewed by the Pathology panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
IGE
Device Class
Class I
Regulation Number
864.4010
Submission Type
Review Panel
PA
Medical Specialty
Pathology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K950560busse hospital disposablesSALINE SOLUTINE, STERILEMay 30, 1995
K842862anatechCB FORMALINAugust 28, 1984