510(k) K880903 ยท LIL Monitor, Penile Tumescence
BARD (R) ESKA ERECTIOMETER
| Applicant | C.R. Bard, Inc., Covington GA, US |
| Decision | Substantially Equivalent, May 6, 1988 |
| Received | Mar 2, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880903
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.