MODEL 480 INFUSION PUMP, MODIFICATION

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 Model 480 Infusion Pump, Modification.

Pre-market Notification Details

Device IDK924868
510k NumberK924868
Device Name:MODEL 480 INFUSION PUMP, MODIFICATION
ClassificationPump, Infusion
Applicant 3M HEALTH CARE, LTD. 3M CENTER, BLDG. 275-3E-08 P.O. BOX 33275 St. Paul,  MN  55133
ContactStan Suedkamp
CorrespondentStan 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 Received1992-09-23
Decision Date1993-06-17

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