510(k) K972136 ยท IZI System, X-Ray, Angiographic
TV MONITOR (P12/17)
| Applicant | Perkins Mfg. Co., Dallas TX, US |
| Decision | Substantially Equivalent, Jun 26, 1997 |
| Received | Jun 6, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972136
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.