Company ยท US
Estech, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1999 to 2013. 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 |
|---|---|---|---|
| Oct 7, 2013 | K133017 | ESTECH COBRA(R) GENESIS BIPOLAR CLAMP Estech, Inc. | GEI |
| Jan 26, 2006 | K053021 | ESTECH CLEARVIEW MV ATRIAL DEPRESSOR Estech, Inc. | DTS |
| Dec 16, 2005 | K052081 | REMOTE ACCESS PERFUSION (RAP) FEMORAL VENOUS CANNULA Estech, Inc. | DWF |
| Sep 13, 2005 | K051749 | COBRA SURGICAL SYSTEM Estech, Inc. | GEI |
| Jul 27, 2004 | K041599 | COBRA ADHERE SURGICAL SYSTEM Estech, Inc. | GEI |
| Oct 22, 2003 | K032632 | REMOTE ACCESS PERFUSION CANNULA LEFT AXILLARY 21 FRENCH Estech, Inc. | DWF |
| Mar 11, 1999 | K990573 | ESTECH ARTERIAL REMOTE ACCESS PERFUSION CANNULA Estech, Inc. | DXC |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||