510(k) K955787 ยท OMB Automatic Event Detection Software For Full-Montage Electroencephalograph
DIGITRACE HOME VIDEO SYSTEM
| Applicant | New England Medical Instruments, Inc., Boston MA, US |
| Decision | Substantially Equivalent, Feb 9, 1996 |
| Received | Dec 21, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955787
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.