510(k) K902472 ยท DRS Transducer, Blood-Pressure, Extravascular
MORSE DT MANIFOLD
| Applicant | North American Instrument Corp., Glens Falls NY, US |
| Decision | Substantially Equivalent, Aug 23, 1990 |
| Received | Jun 4, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902472
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| May 8, 2026 | Medline Industries, LP Namic Preceptor Manifold, custom, Medline Product Number/SKU 64037107; Extravascular blood pressure transducer Open, Classified |
DRS | None listed |
| May 8, 2026 | Medline Industries, LP Namic Preceptor Manifold, custom, Medline Product Number/SKU 64039307; Extravascular blood pressure transducer Open, Classified |
DRS | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.