510(k) K070800 ยท MOL Condom, Synthetic
LIFESTYLES LUBRICATED POLYISOPRENE LATEX MALE CONDOM
| Applicant | Ansell Healthcare Products, LLC, Dothan AL, US |
| Decision | Substantially Equivalent, Mar 6, 2008 |
| Received | Mar 23, 2007 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K070800
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.