510(k) K933334 ยท DQX Wire, Guide, Catheter
MAGIC TORQUE GUIDEWIRE
| Applicant | Boston Scientific Corp, Watertown MA, US |
| Decision | Substantially Equivalent, Jan 26, 1994 |
| Received | Jul 8, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933334
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 20, 2003 | Symbiosis Corp. Medi-Tech Magic Torque Glidex hydrophilic coated guidewire, .035 inch/180 cm and .035 inch/260 cm lengths. Packaged in a sterile pouch and a three pack shelf box. Terminated |
DQX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.