510(k) K952623 ยท GGC Control, Plasma, Abnormal
CRYO CHECK LUPUS PLASMA
| Applicant | Precision Biologicals, Inc., Dartmouth, Nova Scotia, CA |
| Decision | Substantially Equivalent, Nov 6, 1995 |
| Received | Jun 8, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952623
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.