510(k) K930357 ยท KXH Cradle, Patient, Radiologic
ACCESSORY TO UNIVERSAL OCTOPAQUE
| Applicant | Octostop, Inc., Montreal, Qc., CA |
| Decision | Substantially Equivalent, Jul 13, 1993 |
| Received | Jan 26, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930357
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.