Ives MR Conditional Cup Electrode
K-Number: K171102 · 2017-12-21
ApplicantIves Egg Solutions
Decision Date2017-12-21
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
Ives MR Conditional Cup Electrode is a medical device manufactured by Ives Egg Solutions. It received FDA 510(k) clearance on 2017-12-21 under approval number K171102. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Ives MR Conditional Cup Electrode?
Ives MR Conditional Cup Electrode is a medical device that received FDA 510(k) clearance on 2017-12-21. It is manufactured by Ives Egg Solutions. The 510(k) number is K171102.
When was Ives MR Conditional Cup Electrode approved by the FDA?
Ives MR Conditional Cup Electrode received FDA 510(k) clearance on 2017-12-21, under approval number K171102.
What company makes Ives MR Conditional Cup Electrode?
Ives MR Conditional Cup Electrode is manufactured by Ives Egg Solutions.
What is the FDA product code for Ives MR Conditional Cup Electrode?
The FDA product code for Ives MR Conditional Cup Electrode is GXY.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.