Ri Mos. S.R.L.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K992926GINRAM ENDOCIC SINGLE OVAL PORT (MODEL NO. 720195)October 26, 1999
K991895RAMPIPELLA, SINGE PORT (720196) & WEDGE-SHAPED PORT (720217)August 12, 1999
K991827GINRAM SPECUVAG, GINRAM SPECUVAG AS, GINRAM CUSCOVAG, MODELS 720101, 720102, 720103, 720179, 720227,July 19, 1999
K983897CERVICAL ANESTHESIA NEEDLE, CONTRACERVICAL ANESTHESIA NEEDLE, MODEL #'S 720209 30GAU X 4 MM, 720210 February 1, 1999