510(k) K830510 ยท GCY Apparatus, Suction, Single Patient Use, Portable, Nonpowered
BBL STREP GROUPING KIT
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Washington DC, US |
| Decision | Substantially Equivalent, May 2, 1983 |
| Received | Feb 18, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830510
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.