VASCUPUNCTURE PICC GUIDEWIRE

Wire, Guide, Catheter

NEO METRICS, INC.

The following data is part of a premarket notification filed by Neo Metrics, Inc. with the FDA for Vascupuncture Picc Guidewire.

Pre-market Notification Details

Device IDK031652
510k NumberK031652
Device Name:VASCUPUNCTURE PICC GUIDEWIRE
ClassificationWire, Guide, Catheter
Applicant NEO METRICS, INC. 14800 28TH AVENUE NORTH SUITE 150 Plymouth,  MN  55447
ContactGene Champeau
CorrespondentGene Champeau
NEO METRICS, INC. 14800 28TH AVENUE NORTH SUITE 150 Plymouth,  MN  55447
Product CodeDQX  
CFR Regulation Number870.1330 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2003-05-28
Decision Date2003-09-30
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00816840020234 K031652 000
30884908016964 K031652 000
30884908145138 K031652 000

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