Ives MR Conditional Cup Electrode
K-Number: K171102 · 2017-12-21
Device Summary
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. The listed applicant is Ives Egg Solutions. The 510(k) number is K171102.
When did Ives MR Conditional Cup Electrode receive FDA 510(k) clearance?
Ives MR Conditional Cup Electrode received FDA 510(k) clearance on 2017-12-21, under 510(k) number K171102.
Who is the listed applicant for Ives MR Conditional Cup Electrode?
The FDA 510(k) record lists Ives Egg Solutions as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Ives MR Conditional Cup Electrode?
The FDA product code for Ives MR Conditional Cup Electrode is GXY.
Related Devices (Code: GXY)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
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