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MOV — Catheters, Salpingography Class II

FDA Device Classification

Classification Details

Product Code
MOV
Device Class
Class II
Regulation Number
884.4530
Submission Type
Review Panel
OB
Medical Specialty
Obstetrics/Gynecology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K180552cook incorporatedModified Novy Cornual Cannulation SetJuly 12, 2018
K932436echocathECHOMARK INTRAUTERINE GUIDING CATHETERNovember 16, 1995
K953314conceptusCONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEMJuly 28, 1995
K931476cook ob/gynNOVY CORNUAL CANNULATION SETJuly 28, 1995
K931534ovamedOVAMED INTRAUTERINE ACCESS CATHETERJuly 28, 1995