510(k) K033126 ยท LIL Monitor, Penile Tumescence
MONARCH 21 PENILE PLETHYSMOGRAPH SYSTEM
| Applicant | Behavioral Technology, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Oct 29, 2003 |
| Received | Sep 30, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K033126
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.