510(k) K981936 ยท DQX Wire, Guide, Catheter
ABD VARISOFT STEERABLE GUIDE WIRE AND ABD VARISOFT GUIDE WIRE EXTENSION
| Applicant | Advanced Biomedical Devices, Inc., Andover MA, US |
| Decision | Substantially Equivalent, Feb 16, 2000 |
| Received | Jun 2, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981936
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.