510(k) K781333 ยท KGC Tube, Gastro-Enterostomy
CENTRAL CATHETER TRAY
| Applicant | Argon Medical Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 24, 1978 |
| Received | Aug 2, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781333
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 2, 2010 | Argon Medical Devices, Inc CATHETER INTRODUCER KIT PCI KIT/5 REF/REORDER NO. 496185. Disposable Single Use, Rx.. Argon Medical Devices, Inc. 1445 Flat Creek Road Athens, TX 75751. Terminated |
DRE | None listed |
| Jun 2, 2010 | Argon Medical Devices, Inc CATHETER INTRODUCER KIT SPECIAL RIGHT HEART KIT REF/REORDER NO. 496413Y. Disposable Single Use, Rx. Argon Medical Devices, Inc. 1445 Flat Creek Road Athens, TX 75751. Terminated |
KGC | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.