510(k) K860695 ยท KIW Kit, Mycoplasma Detection
GIBCO MYCOTECT KIT (CATALOG NO. 189-5672)
| Applicant | Gibco Laboratories Life Technologies, Inc., Grandisland NY, US |
| Decision | Substantially Equivalent, Mar 12, 1986 |
| Received | Feb 25, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860695
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.