FDA 510(k) Applications Submitted by DONNA A CRAWFORD

FDA 510(k) Number	Submission Date	Device Name	Applicant
K050148	01/24/2005	MENTOR ARIS TRANS-OBTURATOR TAPE AND SURGICAL KIT	MENTOR CORPORATION
K010709	03/09/2001	MENTOR STERILE SALINE MAMMARY VOLUME SIZERS	MENTOR CORP.
K011500	05/16/2001	MENTOR CONTOUR PROFILE TISSUE EXPANDER	MENTOR CORP.
K031767	06/09/2003	MENTOR OBTAPE TRANS-OBTURATOR TAPE	MENTOR CORP.
K042851	10/15/2004	MENTOR OBTAPE TRANS-OBTURATOR SURGICAL KIT	MENTOR CORP.
K050008	01/03/2005	MENTOR SELF-CATH HYDROGEL INTERMITTENT CATHETER	MENTOR CORP.
K980050	01/06/1998	MENTOR SKIN PROTECTION PAD	MENTOR CORP.
K980483	02/09/1998	MENTOR SUSPEND SLING	MENTOR CORP.
K040959	04/13/2004	MENTOR GENESIS PENILE PROSTHESIS	MENTOR CORP.
K981527	04/28/1998	MENTOR PATHWAY INTRODUCER/DILATOR	MENTOR CORP.
K973146	08/22/1997	MENTOR SUPER ABSORBENT DRAPE	MENTOR OPHTHALMICS, INC.
K983065	09/02/1998	MENTOR ULTRASOUND-ASSISTED TISSUE REMOVAL SYSTEM	MENTOR CORP.
K052440	09/06/2005	MENTOR SELF-CATH HYDROGEL INTERMITTENT CATHETER	MENTOR CORPORATION
K993308	10/04/1999	MENTOR EVACARE VAGINAL PESSARIES	MENTOR CORP.
K053296	11/25/2005	MENTOR ARIS SUPRAPUBIC SURGICAL KIT	MENTOR CORPORATION
K974469	11/26/1997	MENTOR PHACOEMULSIFICATION SISTEM REMOTE CONTROL	MENTOR CORP.
K003784	12/07/2000	MENTOR SELF-CATH PLUS	MENTOR CORP.
K053414	12/07/2005	MENTOR NOVASILK MESH	MENTOR CORP.
K003873	12/15/2000	MENTOR SELF-CATH CLOSED SYSTEM	MENTOR CORP.
K004005	12/26/2000	MENTOR ULTRASOUND-ASSISTED TISSUE REMOVAL SYSTEM (CURRENT), MENTOR CONTOUR GENESIS SYSTEM (PROPOSED)	MENTOR CORP.