510(k) K943472 ยท HXB Probe
COHORT AVB RETRACTOR SYSTEM
| Applicant | Cohort Medical Products Group, Inc., Hayward CA, US |
| Decision | Substantially Equivalent, Oct 20, 1994 |
| Received | Jul 19, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943472
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.