510(k) K003442 ยท HLX Photostimulator, Ac-Powered
MODIFICATION TO EDI VERIS SYSTEM
| Applicant | Electro-Diagnostic Imaging, Inc., Los Altos CA, US |
| Decision | Substantially Equivalent, May 4, 2001 |
| Received | Nov 6, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003442
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.