510(k) K840144 ยท FCG Biopsy Needle
YAG LASER 8000 GASTROINTESTINAL BLEE
| Applicant | Cooper Medical Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, May 18, 1984 |
| Received | Jan 13, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840144
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.