510(k) K822919 ยท HLX Photostimulator, Ac-Powered
5010 VISUSTIM
| Applicant | Life-Tech Intl., Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 28, 1982 |
| Received | Oct 1, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K822919
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.