510(k) K032156 ยท IYE Accelerator, Linear, Medical
ACCUFIX RADIOLUCENT PELVIS AND BELLY BOARDS, ACCUFIX CANTILEVER HEAD BOARD WITH SHOULDER DEPRESSION, ACCUFIX RADIOLUCENT
| Applicant | Wfr/Aquaplast Corp., Wyckoff NJ, US |
| Decision | Substantially Equivalent, Sep 2, 2003 |
| Received | Jul 14, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032156
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.