Ri Mos. S.R.L. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ri Mos. S.R.L. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Ri Mos. S.R.L. has 4 FDA 510(k) cleared medical devices. Based in Concord, US.
Historical record: 4 cleared submissions from 1999 to 1999. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Ri Mos. S.R.L. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ri Mos. S.R.L.
4 devices
Cleared
Oct 26, 1999
GINRAM ENDOCIC SINGLE OVAL PORT (MODEL NO. 720195)
Obstetrics & Gynecology
56d
Cleared
Aug 12, 1999
RAMPIPELLA, SINGE PORT (720196) & WEDGE-SHAPED PORT (720217)
Obstetrics & Gynecology
70d
Cleared
Jul 19, 1999
GINRAM SPECUVAG, GINRAM SPECUVAG AS, GINRAM CUSCOVAG, MODELS 720101, 720102,...
Obstetrics & Gynecology
52d
Cleared
Feb 01, 1999
CERVICAL ANESTHESIA NEEDLE, CONTRACERVICAL ANESTHESIA NEEDLE, MODEL #'S...
Obstetrics & Gynecology
90d