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LDX — Fixative, Metallic Containing Class I

FDA Device Classification

Classification Details

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

Recent 510(k) Clearances

K-Number	Applicant	Device Name	Date
K882874	anatech	ZINC FORMALIN	July 28, 1988