510(k) K941959 ยท HCC Device, Biofeedback
VERSATELL; VERSATELL-S
| Applicant | Progressive Concepts, Inc., Denton MD, US |
| Decision | Substantially Equivalent, Jun 21, 1995 |
| Received | Apr 22, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K941959
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.