510(k) K882311 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
SHIMADZU LATERAL C-ARM MH-31
| Applicant | Shimadzu Precision Instruments, Inc., Torrance CA, US |
| Decision | Substantially Equivalent, Sep 14, 1988 |
| Received | Jun 3, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882311
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.