510(k) K940128 ยท LIL Monitor, Penile Tumescence
CAT-400UL PENILE PLETHYSMOGRAPH
| Applicant | Farrall Instruments, Inc., Grand Island NE, US |
| Decision | Substantially Equivalent, Jan 10, 1995 |
| Received | Jan 10, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K940128
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.