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FBM — Cannula And Trocar, Suprapubic, Non-Disposable Class I

FDA Device Classification

Classification Details

Product Code
FBM
Device Class
Class I
Regulation Number
876.5090
Submission Type
Review Panel
GU
Medical Specialty
Gastroenterology, Urology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K960400snowden-pencerDIAMOND-TOUCH AND MICRO DIAMOND-TOUCH INSTRUMENTS/DIAMOND-LINE INSTRUMENTS/DIAMOMarch 12, 1996
K932021core dynamicsENTREE CANNULA FASCIA ANCHORSJanuary 11, 1994
K911813core dynamicsENTREE CANNULAJuly 19, 1991
K900962solos endoscopyGS-4300 CANNULA AND TROCAR, 5.5MMApril 18, 1990
K900964solos endoscopyCANNULA AND TROCAR, 11MMApril 18, 1990
K900965solos endoscopyGS-4550 TROCAR ONLY, 11MMApril 18, 1990
K900955solos endoscopyGS-4000 REDUCER SLEEVE, 11MM TO 5MMApril 18, 1990
K900961solos endoscopyGS-4100 REDUCER SLEEVE, 5MM TO 3MMApril 18, 1990
K900963solos endoscopyGS-4350 TROCAR ONLY, 5.5MMApril 18, 1990