FDA 510(k) Applications for Medical Device Product Code: HTD (Forceps)

FDA 510(k) Applications for Medical Device Product Code "HTD"
(Forceps)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K051281	E.D.MEDICAL LTD.	THE NEEDLE CATCHER	09/08/2005
K974595	TITAN MFG., INC.	CUSHING BAYONET, INSULATED BIPOLAR FORCEP	06/24/1998
K974594	TITAN MFG., INC.	SEMKIN BIPOLAR FORCEP	06/24/1998
K974593	TITAN MFG., INC.	SEMKIN INSULATED BIPOLAR FORCEP	06/24/1998