510(k) K912747 ยท HJN Transilluminator, Battery-Powered
LULMITEX NEONATAL TRANSILLUMINATOR
| Applicant | Lumitex, Inc., Cleveland OH, US |
| Decision | Substantially Equivalent, Dec 24, 1991 |
| Received | Jun 21, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912747
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.