510(k) K993909 ยท LKY Device, External Penile Rigidity
NANMA VACUUM PUMP
| Applicant | Nanma Mfg Co., Ltd., Crofton MD, US |
| Decision | Substantially Equivalent, Jul 19, 2000 |
| Received | Nov 17, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993909
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.