LDW — Fixative, Acid Containing Class I

FDA Device Classification

Classification Details

Product Code
LDW
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
K883062alpha-tec systemsATS SCHAUDINN'S FIXATIVE W/ACETIC ACIDAugust 4, 1988
K842923e k indPICRIC ACID 1% W/VSeptember 11, 1984
K842922e k indPICRIC ACID SATURATED SOLUTIONSeptember 7, 1984
K831058american micro scanSAF FIXATIVEJune 8, 1983