Company ยท US
Summit Doppler Systems, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2003 to 2011. Name variants (Inc, Corp, punctuation) are merged.
7510(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 |
|---|---|---|---|
| Feb 15, 2011 | K103693 | VANTAGE ABI Summit Doppler Systems, Inc. | DXN |
| Aug 19, 2010 | K101816 | STN PROBE Summit Doppler Systems, Inc. | ITX |
| Dec 24, 2009 | K093393 | LIFEDOP MODEL 300ABI Summit Doppler Systems, Inc. | JAF |
| Mar 31, 2009 | K090499 | LIFEDOP MODEL, L350R Summit Doppler Systems, Inc. | MAA |
| Dec 19, 2006 | K063600 | VISTA AVS Summit Doppler Systems, Inc. | JAF |
| Apr 10, 2006 | K060410 | ECHOHEART TRANSVAGINAL DOPPLER PROBE Summit Doppler Systems, Inc. | HEK |
| Jan 3, 2003 | K024197 | LIFEDOP DOPPLER Summit Doppler Systems, Inc. | KNG |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||