KQS — Table, Cystometric, Non-Electric And Accessories Class I

FDA Device Classification

Classification Details

Product Code
KQS
Device Class
Class I
Regulation Number
876.4890
Submission Type
Review Panel
GU
Medical Specialty
Gastroenterology, Urology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K955019dornier medtech americaUROTRACT IDecember 6, 1995
K872022oec-diasonicsUROVIEWJuly 16, 1987
K864846american sterilizerRADIOGRAPHIC - LEG SECTIONDecember 24, 1986
K860040mallinckrodt groupHYDRAJUST III UROLOGICAL TABLEFebruary 10, 1986
K852127american sterilizerAMSCO URO-ENDO MOBILE TABLEAugust 8, 1985
K801723siemensUR 150-UR 150TAugust 13, 1980
K791699sybronHYDRADJUST II UROLOGICAL TABLEOctober 22, 1979
K760522mallinckrodt groupTABLE, UROSURGICALDecember 16, 1976