510(k) K883689 ยท JPA System, Multipurpose For In Vitro Coagulation Studies
ORTHO OWREN'S BUFFER
| Applicant | Ortho Diagnostic Systems, Inc., Raritan NJ, US |
| Decision | Substantially Equivalent, Nov 1, 1988 |
| Received | Aug 29, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883689
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.