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KDM — Sigmoidoscope, Rigid, Non-Electrical Class II

FDA Device Classification

Classification Details

Product Code: KDM
Device Class: Class II
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
K070915	sapimed	SAPIMED DISPOSABLE SIGMOIDOSCOPE	July 6, 2007