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GPM — Antiserum, Murine Typhus Fever Class I

FDA Device Classification

Classification Details

Product Code: GPM
Device Class: Class I
Regulation Number: 866.3500
Submission Type
Review Panel: MI
Medical Specialty: Microbiology
Implant: No

Recent 510(k) Clearances

K-Number	Applicant	Device Name	Date
K860557	health research	LATEX R. TYPHI	April 21, 1986