510(k) K882975 ยท FMF Syringe, Piston
RE-VENT ARTERIAL BLOOD SAMPLER AND/OR BIOSAMPLER
| Applicant | Richmann Laboratories, Lake Park FL, US |
| Decision | Substantially Equivalent, Jan 25, 1989 |
| Received | Jul 15, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882975
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.