510(k) K840500 ยท JPH Test, Erythrocyte Sedimentation Rate
SEDIPLAST
| Applicant | Precision Technology, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 21, 1984 |
| Received | Feb 6, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840500
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 7, 2026 | POLYMEDCO, INC. / POLYMEDCO CANCER DIAGNOSTIC PRODUCTS, LLC SEDIPLAST;
Model/Catalog Numbers: S-100 and S-1000; Open, Classified |
JPH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.