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.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list American I.V. Products with 8 510(k) clearances. The most recent is a 510(k) clearance dated Dec 18, 2014: SMART LABEL, PROPOFOL.
| Dec 18, 2014 | SMART LABEL, PROPOFOLK142333 · MRZ | 510(k) clearances |
| Apr 12, 2012 | PATIENT CONTROLLED ANALGESIA (PCA) BUTTON CABLEK120209 · MRZ | 510(k) clearances |
| Mar 27, 2007 | ECG CABLES, TRUNK AND PATIENT LEAD WIRESK070232 · DSA | 510(k) clearances |
| Mar 19, 2007 | CLINICAL ELECTRONIC THERMOMETER, MODELS TP11403 THROUGH TP11413K070342 · FLL | 510(k) clearances |
| Sep 29, 2006 | PULSE OXIMETER ADAPTER CABLESK052544 · DQA | 510(k) clearances |
| Sep 14, 2004 | TRANSDUCERS FOR ULTRASOUND AND TOCODYNAMOMETER FETAL MONITORINGK040392 · HFM | 510(k) clearances |
| Aug 16, 2004 | TRANSDUCER FOR ULTRASOUND FETAL MONITORING, MODELS FM10833 AND FM10834K040819 · HGM | 510(k) clearances |
| Oct 9, 2003 | REPLACEMENT PUMP HEAD DOOR ASSEMBLY, P1, MODEL BX10468, REPLACEMENT PUMP HEAD DOOR ASSEMBLY, P2, MODEL BX10469K032789 · FRN | 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
