ClearanceBrief
Company ยท US

American I.V. Products, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2003 to 2012. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DQAOximeter1
DSACable, Transducer And Electrode, Patient, (Including Connector)1
FLLContinuous Measurement Thermometer1
FRNPump, Infusion1
HFMMonitor, Uterine Contraction, External (For Use In Clinic)1
HGMSystem, Monitoring, Perinatal1
MRZAccessories, Pump, Infusion1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 12, 2012K120209PATIENT CONTROLLED ANALGESIA (PCA) BUTTON CABLE
American I.V. Products, Inc.
MRZ
Mar 27, 2007K070232ECG CABLES, TRUNK AND PATIENT LEAD WIRES
American I.V. Products, Inc.
DSA
Mar 19, 2007K070342CLINICAL ELECTRONIC THERMOMETER, MODELS TP11403 THROUGH TP11413
American I.V. Products, Inc.
FLL
Sep 29, 2006K052544PULSE OXIMETER ADAPTER CABLES
American I.V. Products, Inc.
DQA
Sep 14, 2004K040392TRANSDUCERS FOR ULTRASOUND AND TOCODYNAMOMETER FETAL MONITORING
American I.V. Products, Inc.
HFM
Aug 16, 2004K040819TRANSDUCER FOR ULTRASOUND FETAL MONITORING, MODELS FM10833 AND FM10834
American I.V. Products, Inc.
HGM
Oct 9, 2003K032789REPLACEMENT PUMP HEAD DOOR ASSEMBLY, P1, MODEL BX10468, REPLACEMENT PUMP HEAD DOOR ASSEMBLY, P2, MODEL BX10469
American I.V. Products, Inc.
FRN

Latest recalls

DateFirm and productCodeLinked 510(k)
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