FDA 510(k)

Magic3 Go Intermittent Urinary Catheter

K-Number: K172247 · 2017-09-20

Decision Date2017-09-20

Product CodeEZD

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

Magic3 Go Intermittent Urinary Catheter is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2017-09-20 under 510(k) 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. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K172247.

When did Magic3 Go Intermittent Urinary Catheter receive FDA 510(k) clearance?

Magic3 Go Intermittent Urinary Catheter received FDA 510(k) clearance on 2017-09-20, under 510(k) number K172247.

Who is the listed applicant for Magic3 Go Intermittent Urinary Catheter?

The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

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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Related Devices (Code: 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.