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FFI — System, Alarm, Electrosurgical Class II

FDA Device Classification

Classification Details

Product Code: FFI
Device Class: Class II
Regulation Number: 876.4300
Submission Type
Review Panel: GU
Medical Specialty: Gastroenterology, Urology
Implant: No

Recent 510(k) Clearances

K-Number	Applicant	Device Name	Date
K843214	akron city hospital	EPHAR	November 29, 1984