FDA 510(k) Applications Submitted by ANDREW I 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 |
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