510(k) K052929 ยท LIL Monitor, Penile Tumescence
PREFTEST PROFESSIONAL SUITE
| Applicant | Limestone Technologies, Inc., Dundas, CA |
| Decision | Substantially Equivalent, Apr 26, 2006 |
| Received | Oct 19, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052929
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.