510(k) K834168 ยท JZD Snare, Ear
FIBRINOGEN UPTAKE SYS -VARIOUS MODELS
| Applicant | Canberra Industries, Inc., Meriden CT, US |
| Decision | Substantially Equivalent, Dec 29, 1983 |
| Received | Nov 4, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K834168
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.