510(k) K020292 ยท LKF Cannula, Manipulator/Injector, Uterine
UTERINE INJECTOR
| Applicant | Catheter Research, Inc., Indianapolis IN, US |
| Decision | Substantially Equivalent, Apr 17, 2002 |
| Received | Jan 28, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020292
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 1, 2006 | Catheter Research, Inc Zinnanti Injector - 2.0; Size 2.0 mm, Length 23 cm, latex free, single-use, sterile. For in-office or hospital use when efficient sealing of the uterine cervix is required for the injection of liquid Terminated |
LKF | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.