MODEL 5866-37M 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 5866-37m Lead Adaptor Kit.

Pre-market Notification Details

Device IDK904575
510k NumberK904575
Device Name:MODEL 5866-37M LEAD ADAPTOR KIT
ClassificationPacemaker Lead Adaptor
Applicant MEDTRONIC VASCULAR 7000 CENTRAL AVE. N.E. Minneapolis,  MN  55432
ContactNorsted, Phd
CorrespondentNorsted, Phd
MEDTRONIC VASCULAR 7000 CENTRAL AVE. N.E. Minneapolis,  MN  55432
Product CodeDTD  
CFR Regulation Number870.3620 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1990-10-09
Decision Date1991-02-01

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00613994897923 K904575 000

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