Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of BaxterLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list American McGaw with 13 510(k) clearances. The most recent is a 510(k) clearance dated Nov 12, 1985: MCGAW/DROP WATCH FLOW MONITOR.
| Nov 12, 1985 | MCGAW/DROP WATCH FLOW MONITORK853549 · FLN | 510(k) clearances |
| Jan 14, 1985 | ADD-A-VIAL SOLUTION TRANSFER DEVICEK843639 · LHI | 510(k) clearances |
| Nov 28, 1984 | MIXING CONTAINERK843954 · KPE | 510(k) clearances |
| Jun 1, 1984 | ACCUPRO ENTERAL FEEDING PUMPK841729 · FRN | 510(k) clearances |
| Mar 6, 1984 | CONCENTRATED PLATELET ADMIN. SETK840212 · FPA | 510(k) clearances |
| Mar 6, 1984 | PAB IV CONTAINERK840388 · KPE | 510(k) clearances |
| Jun 24, 1983 | CAPD - CATHETER ADAPTERK831716 · FKX | 510(k) clearances |
| Dec 30, 1982 | ETHYLENE OXIDE STERILIZ. PARAMETRIC REL.K822240 · KFX | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
