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FEJ — Attachment, Binocular, For Endoscope Class I

FDA Device Classification

Classification Details

Product Code: FEJ
Device Class: Class I
Regulation Number: 876.1500
Submission Type
Review Panel: GU
Medical Specialty: Gastroenterology, Urology
Implant: No

Recent 510(k) Clearances

K-Number	Applicant	Device Name	Date
K840837	manico	TBI TRAINER	March 25, 1985