510(k) K992145 ยท FPA Set, Administration, Intravascular
ECOMED SCALP VEIN SET
| Applicant | Greiner Meditech, Inc., Bel Air MD, US |
| Decision | Substantially Equivalent, Oct 14, 1999 |
| Received | Jun 24, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992145
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 29, 2004 | Greiner VACUETTE North America Holdex + Butterfly, Blood Collection Set, Single use only. Sterile, Manufactured by : CA Greiner & Sohne Gmbh, Bad Haller Str. 32, A-4550 Kremsmunster, Austria. Terminated |
FPA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.