510(k) K926222 ยท JPA System, Multipurpose For In Vitro Coagulation Studies
OWREN'S VERONAL BUFFER #5375 & FIBRONOGEN KIT#5376
| Applicant | Helena Laboratories, Beaumont TX, US |
| Decision | Substantially Equivalent, Feb 12, 1993 |
| Received | Dec 10, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926222
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.