510(k) K862848 ยท GWC Antisera, All Types, Streptococcus Pneumoniae
LKB ULTROBACT (TM) PNEUMOCOCCUS KIT; 2321-110
| Applicant | Lkb Instruments, Inc., Gaithersburg MD, US |
| Decision | Substantially Equivalent, Dec 18, 1986 |
| Received | Jul 29, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862848
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.