Magic3 Go Intermittent Urinary Catheter
K-Number: K172247 · 2017-09-20
ApplicantC.R. Bard, Inc.
Decision Date2017-09-20
Product CodeEZD
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Magic3 Go Intermittent Urinary Catheter is a medical device manufactured by C.R. Bard, Inc.. It received FDA 510(k) clearance on 2017-09-20 under approval number K172247. The device is classified under product code EZD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Magic3 Go Intermittent Urinary Catheter?
Magic3 Go Intermittent Urinary Catheter is a medical device that received FDA 510(k) clearance on 2017-09-20. It is manufactured by C.R. Bard, Inc.. The 510(k) number is K172247.
When was Magic3 Go Intermittent Urinary Catheter approved by the FDA?
Magic3 Go Intermittent Urinary Catheter received FDA 510(k) clearance on 2017-09-20, under approval number K172247.
What company makes Magic3 Go Intermittent Urinary Catheter?
Magic3 Go Intermittent Urinary Catheter is manufactured by C.R. Bard, Inc..
What is the FDA product code for Magic3 Go Intermittent Urinary Catheter?
The FDA product code for Magic3 Go Intermittent Urinary Catheter is EZD.
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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.