MODEL 2872 BIPOLAR LEAD ADAPTOR KIT

Pacemaker Lead Adaptor

MEDTRONIC VASCULAR

The following data is part of a premarket notification filed by Medtronic Vascular with the FDA for Model 2872 Bipolar Lead Adaptor Kit.

Pre-market Notification Details

Device IDK982220
510k NumberK982220
Device Name:MODEL 2872 BIPOLAR LEAD ADAPTOR KIT
ClassificationPacemaker Lead Adaptor
Applicant MEDTRONIC VASCULAR 7000 CENTRAL AVE. NE Minneapolis,  MN  55432 -3576
ContactBrian J Edwards
CorrespondentBrian J Edwards
MEDTRONIC VASCULAR 7000 CENTRAL AVE. NE Minneapolis,  MN  55432 -3576
Product CodeDTD  
CFR Regulation Number870.3620 [🔎]
DecisionSe Subject To Tracking Reg (ST)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1998-06-24
Decision Date1998-10-15
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00681490064583 K982220 000

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