510(k) K873834 ยท HCC Device, Biofeedback
INET MODEL BIOVISION
| Applicant | Inet Corp., Newark CA, US |
| Decision | Substantially Equivalent, Mar 24, 1988 |
| Received | Sep 21, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873834
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.