510(k) K072320 ยท FMI Needle, Hypodermic, Single Lumen
GREINER VACUETTE QUICKSHIELD COMPLETE
| Applicant | Greiner Bio-One North America, Inc., Baldwin MD, US |
| Decision | Substantially Equivalent, Sep 14, 2007 |
| Received | Aug 20, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K072320
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 3, 2012 | Greiner Bio-One North America, Inc. Vacuette Quickshield Complete Plus, 21G x 1 (0.8 x 25 mm), Greiner bio-one.
The Quick shield Complete Plus is intended to be used only with Vacuette Blood collection Tubes as a system in routine veni Terminated |
FMI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.