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FHP — Needle, Pneumoperitoneum, Simple Class II

FDA Device Classification

Classification Details

Product Code
FHP
Device Class
Class II
Regulation Number
876.1500
Submission Type
Review Panel
GU
Medical Specialty
Gastroenterology, Urology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K910855symbiosisENDOPATH VERESS NEEDLEApril 18, 1991
K860102endotherapeuticsMOD. ENDONEEDLE SINGLE-USE PNEUMOPERITONEUM NEEDLEFebruary 12, 1986