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LIA — Antigens, All Groups, Shigella Spp. Class II

FDA Device Classification

Classification Details

Product Code: LIA
Device Class: Class II
Regulation Number: 866.3660
Submission Type
Review Panel: MI
Medical Specialty: Microbiology
Implant: No

Recent 510(k) Clearances

K-Number	Applicant	Device Name	Date
K813191	lab ability	SHIGELLA SERA-CHEK	December 3, 1981