510(k) K020082 ยท LKY Device, External Penile Rigidity
ERECAID CLASSIC SYSTEM; ERECAID ESTEEM MANUAL SYSTEM; ERECAID ESTEEM BATTERY SYSTEM
| Applicant | Endocare, Inc., Eden Prairie MN, US |
| Decision | Substantially Equivalent, Feb 5, 2002 |
| Received | Jan 10, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K020082
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.