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GPP — Antiserum, Rocky Mountain Spotted Fever Class I

FDA Device Classification

Classification Details

Product Code: GPP
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
K843794	health research	LATEX-R RICKETTSII	January 4, 1985