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FIW — Alarm, Pillow Pressure Class II

FDA Device Classification

Classification Details

Product Code: FIW
Device Class: Class II
Regulation Number: 876.5820
Submission Type
Review Panel: GU
Medical Specialty: Gastroenterology, Urology
Implant: No

Recent 510(k) Clearances

K-Number	Applicant	Device Name	Date
K772355	cordis	BLOOD LINE COMP. NEG. PRESS. PILLOW	January 26, 1978