510(k) K912073 ยท LMC Camera, Multi Format, Radiological
POLAROID HELIOS LASER IMAGER
| Applicant | Polaroid Medical Corp., Washington DC, US |
| Decision | Substantially Equivalent, Aug 28, 1991 |
| Received | May 10, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912073
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.