FDA 510(k) Applications Submitted by ANDREW SEALFON

FDA 510(k) Number	Submission Date	Device Name	Applicant
K102512	09/01/2010	RMS SUBCUTANEOUS NEEDLE SET	REPRO-MED SYSTEMS, INC.
K980948	03/13/1998	VED VALU- VACUUM ERECTION DEVICE	MISSION PHARMACAL COMP
K981506	04/27/1998	RESTORE VACUUM ERECTION DEVICE, CONFIDE VACUUM ERECTION DEVICE, PEP (PENILE ERECTION PROGRAM), RELY VACUUM ERECTION DEV)	REPRO-MED SYSTEMS, INC.
K122404	08/07/2012	MODEL NUMBER: RMS1-2604, RMS1-2614, RMS1-2404, RMS1-2414, RMS2-2604, RMS2-2614, RMS2-2404, RMS2-2414, RMS3-2604, RMS3-26	REPRO-MED SYSTEMS, INC. DBA RMS MEDICAL PRODUCTS