510(k) K982559 ยท DQX Wire, Guide, Catheter
GUIDEWIRE
| Applicant | Galt Medical Corp., Garland TX, US |
| Decision | Substantially Equivalent, Feb 1, 1999 |
| Received | Jul 23, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982559
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| May 7, 2025 | Galt Medical Corporation GALT Guidewire
REF SGW-051-07
Guidewires are intended for use in percutaneous procedures, to introduce and position catheters and other interventional devices within the Coronary and peripheral vascu Open, Classified |
DQX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.