510(k) K990707 ยท DQY Catheter, Percutaneous
MEDTRONIC 5F & 9F ZUMA GUIDING CATHETERS
| Applicant | Medtronics Interventional Vascular, Danvers MA, US |
| Decision | Substantially Equivalent, Mar 22, 1999 |
| Received | Mar 4, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K990707
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 8, 2011 | Medtronic Vascular Medtronic 6F Zuma Guide Catheter with AL 1.5 Curve with side holes
Catalog Number: Z26AL15SH
The Medtronic Guiding Catheter is designed to provide a pathway through which therapeutic devices are in Terminated |
DQY | None listed |
| Jun 1, 2006 | Medtronic, Inc. 5F ZUMA SR3.0
CATHETER ZM5SR30 Z2 5F 100CM SR30 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are introduced into the coronary or periphe Terminated |
DQY | None listed |
| Jun 1, 2006 | Medtronic, Inc. ZM5SR35 5F ZUMA SR3.5
CATHETER ZM5SR35 Z2 5F 100CM SR35 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are introduced into the coronary or Terminated |
DQY | None listed |
| Jun 1, 2006 | Medtronic, Inc. 5F ZUMA SR4.0
CATHETER ZM5SR40 Z2 5F 100CM SR40 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are introduced into the coronary or periphe Terminated |
DQY | None listed |
| Jun 1, 2006 | Medtronic, Inc. 5F ZUMA SR5.0 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are introduced into the coronary or peripheral vascular system.
Product Cod Terminated |
DQY | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.