Home / Device Classification / HTD

HTD — Forceps Class I

FDA Device Classification

Classification Details

Product Code
HTD
Device Class
Class I
Regulation Number
878.4800
Submission Type
Review Panel
SU
Medical Specialty
General, Plastic Surgery
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K051281e.d.medicalTHE NEEDLE CATCHERSeptember 8, 2005
K974594titan mfgSEMKIN BIPOLAR FORCEPJune 24, 1998
K974593titan mfgSEMKIN INSULATED BIPOLAR FORCEPJune 24, 1998
K974595titan mfgCUSHING BAYONET, INSULATED BIPOLAR FORCEPJune 24, 1998
K913964marlo surgical technologyMARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPSOctober 23, 1991
K911180northgate technologiesCLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPSMarch 29, 1991
K895212instruments of swedenTIK EXTRAKTORSeptember 27, 1989
K890373kinetic medical productsHEMORRHOIDAL FORCEPSFebruary 3, 1989
K890369kinetic medical productsGALL STONE FORCEPSFebruary 3, 1989
K890258kinetic medical productsBONE CUTTING FORCEPS, SINGLE-ACTIONJanuary 27, 1989
K890226kinetic medical productsSURGICAL FORCEPSJanuary 27, 1989
K890234kinetic medical productsSUTURE CLIP REMOVERJanuary 27, 1989
K890246kinetic medical productsARTERY FORCEPSJanuary 27, 1989
K890263kinetic medical productsCILIA FORCEPSJanuary 27, 1989
K890257kinetic medical productsBONE CUTTING FORCEPS, DOUBLE-ACTIONJanuary 27, 1989
K890238kinetic medical productsCATHETER FORCEPSJanuary 27, 1989
K890213kinetic medical productsMICROSURGICAL FORCEPSJanuary 27, 1989
K890260kinetic medical productsBONE SHEARSJanuary 27, 1989
K890262kinetic medical productsLUNG FORCEPSJanuary 27, 1989
K890259kinetic medical productsRIB SHEARSJanuary 27, 1989