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FDP — Apparatus, Pneumoperitoneum, Automatic Class II

FDA Device Classification

Classification Details

Product Code: FDP
Device Class: Class II
Regulation Number: 876.1500
Submission Type
Review Panel: SU
Medical Specialty: Gastroenterology, Urology
Implant: No

Recent 510(k) Clearances

K-Number	Applicant	Device Name	Date
K910875	ethicon	ENDOPATH DISPOSABLE PNEUMOPERITONEUM NEEDLE	March 19, 1991