510(k) K910833 ยท GSA Antisera, All Mycoplasma Spp.
COLOR VUE TM- MYCOPLASMA PNEUMONIAE
| Applicant | Seradyn, Inc., Indianapolis IN, US |
| Decision | Substantially Equivalent, Jun 24, 1991 |
| Received | Feb 27, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910833
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.