510(k) K831252 ยท LIL Monitor, Penile Tumescence
TUMISTORE RECORDER 1311
| Applicant | Life-Tech Intl., Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 18, 1983 |
| Received | Apr 18, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831252
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.