ClearanceBrief
Company ยท US

Advanced Infusion, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1999 to 2008. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
MEBPump, Infusion, Elastomeric5
MEDSterilant, Medical Devices1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Feb 19, 2008K071532ALPHA INFUSION PUMP, MODEL A200, A450
Advanced Infusion, Inc.
MEB
Oct 18, 2006K061661STA CATH ATTACHABLE INFISION CATHETER, MODEL STA20
Advanced Infusion, Inc.
MEB
Jul 3, 2006K061356POLYURETHANE INFUSION CATHETER, ALPHA CATH, MODEL PAC20, AND POLYURETHANE INFUSION CATHETER, MULTI DRIP, MODEL PMD20-6
Advanced Infusion, Inc.
MED
Aug 31, 2004K042246MULTI-DRIP INFUSION CATHETER
Advanced Infusion, Inc.
MEB
Aug 12, 2002K021964ALPHA INFUSION PUMP AND CATHETERS
Advanced Infusion, Inc.
MEB
Oct 27, 1999K992551ALPHA INFUSION PUMP
Advanced Infusion, Inc.
MEB

Latest recalls

DateFirm and productCodeLinked 510(k)
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