Ri Mos. S.R.L.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K992926 | GINRAM ENDOCIC SINGLE OVAL PORT (MODEL NO. 720195) | HHK | 1999-10-26 | View |
| 510(k) | K991895 | RAMPIPELLA, SINGE PORT (720196) & WEDGE-SHAPED PORT (720217) | HHK | 1999-08-12 | View |
| 510(k) | K991827 | GINRAM SPECUVAG, GINRAM SPECUVAG AS, GINRAM CUSCOVAG, MODELS 720101, 720102, 720103, 720179, 720227, 720043 | HIB | 1999-07-19 | View |
| 510(k) | K983897 | CERVICAL ANESTHESIA NEEDLE, CONTRACERVICAL ANESTHESIA NEEDLE, MODEL #'S 720209 30GAU X 4 MM, 720210 30GAU X 6MM, 720208G | HEE | 1999-02-01 | View |
No matching devices.
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