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FDA 510(k)

KIMBERLY-CLARK MIC-KEY LOW PROFILE GASTROSTOMY TUBE

K-Number: K043114 · 2004-12-10

ApplicantKimberly-Clark Corp.
Decision Date2004-12-10
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KIMBERLY-CLARK MIC-KEY LOW PROFILE GASTROSTOMY TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Kimberly-Clark Corp.. It received FDA 510(k) clearance on 2004-12-10 under 510(k) number K043114. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KIMBERLY-CLARK MIC-KEY LOW PROFILE GASTROSTOMY TUBE?

KIMBERLY-CLARK MIC-KEY LOW PROFILE GASTROSTOMY TUBE is a medical device that received FDA 510(k) clearance on 2004-12-10. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K043114.

When did KIMBERLY-CLARK MIC-KEY LOW PROFILE GASTROSTOMY TUBE receive FDA 510(k) clearance?

KIMBERLY-CLARK MIC-KEY LOW PROFILE GASTROSTOMY TUBE received FDA 510(k) clearance on 2004-12-10, under 510(k) number K043114.

Who is the listed applicant for KIMBERLY-CLARK MIC-KEY LOW PROFILE GASTROSTOMY TUBE?

The FDA 510(k) record lists Kimberly-Clark Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KIMBERLY-CLARK MIC-KEY LOW PROFILE GASTROSTOMY TUBE?

The FDA product code for KIMBERLY-CLARK MIC-KEY LOW PROFILE GASTROSTOMY TUBE is KNT.

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Related Devices (Code: KNT)

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.

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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.

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