FDA 510(k) Applications Submitted by JOHN G MOULDEN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K960388	01/26/1996	DYNAREX NON-WOVEN SPONGE	DYNAREX CORP.
K991694	05/18/1999	DYNAREX DRAIN SPONGE	DYNAREX CORP.
K991695	05/18/1999	DYNAREX NON-WOVEN SPONGE	DYNAREX CORP.
K983348	09/23/1998	DYNAREX TRACHEOSTOMY SPONGE	DYNAREX CORP.