AVI MODEL 3000 INFUSION PUMP

Pump, Infusion

3M HEALTH CARE, LTD.

The following data is part of a premarket notification filed by 3m Health Care, Ltd. with the FDA for Avi Model 3000 Infusion Pump.

Pre-market Notification Details

Device IDK920588
510k NumberK920588
Device Name:AVI MODEL 3000 INFUSION PUMP
ClassificationPump, Infusion
Applicant 3M HEALTH CARE, LTD. 3M CENTER, BLDG. 275-3E-08 P.O. BOX 33275 St. Paul,  MN  55133
ContactStanley J Suedkamp
CorrespondentStanley J Suedkamp
3M HEALTH CARE, LTD. 3M CENTER, BLDG. 275-3E-08 P.O. BOX 33275 St. Paul,  MN  55133
Product CodeFRN  
CFR Regulation Number880.5725 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1992-02-10
Decision Date1992-04-06

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