510(k) K943801 ยท FCS Light, Catheter, Fiberoptic, Glass, Ureteral
URIGLOW TRANSILLUMINATING URETERIC STENT MODEL
| Applicant | Rocket of London, Ltd., Tyne & Wear, GB |
| Decision | Substantially Equivalent, Aug 15, 1995 |
| Received | Aug 3, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943801
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.