510(k) K823131 ยท KQG Instrument, Coagulation
KOAGULAB 40-A AUTOMATED COAGULATION SYS
| Applicant | Ortho Diagnostic Systems, Inc., Carpinteria CA, US |
| Decision | Substantially Equivalent, Dec 9, 1982 |
| Received | Oct 25, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823131
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.