Company ยท US
Siemens Medical Corp.
FDA 510(k) clearances and medical device recalls filed under this name, 1999 to 2001. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 27, 2001 | K012202 | NUMARIS 4VA15A Siemens Medical Corp. | LNH |
| Mar 30, 2001 | K010721 | AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEM Siemens Medical Corp. | IZI |
| Aug 10, 2000 | K994231 | SIEMENS INTEGRATED OPERATING SYSTEM (SIOS) Siemens Medical Corp. | ODA |
| Jan 14, 2000 | K994316 | MAGNETOM OPEN VIVA WITH PERMANENT MAGNET Siemens Medical Corp. | LNH |
| Mar 12, 1999 | K984634 | 3D-ANGIO Siemens Medical Corp. | JAK |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||