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FDA 510(k)

MIC-KEY SF LOW PROFILE GASTROSTOMY TUBE AND ACCESSORIES

K-Number: K122653 · 2013-06-26

Decision Date2013-06-26
Product CodeKNT
Advisory CommitteeGU
DecisionUnknown

Device Summary

MIC-KEY SF LOW PROFILE GASTROSTOMY TUBE AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Kimberly-Clark Corporation. It received FDA 510(k) clearance on 2013-06-26 under 510(k) number K122653. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MIC-KEY SF LOW PROFILE GASTROSTOMY TUBE AND ACCESSORIES?

MIC-KEY SF LOW PROFILE GASTROSTOMY TUBE AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 2013-06-26. The listed applicant is Kimberly-Clark Corporation. The 510(k) number is K122653.

When did MIC-KEY SF LOW PROFILE GASTROSTOMY TUBE AND ACCESSORIES receive FDA 510(k) clearance?

MIC-KEY SF LOW PROFILE GASTROSTOMY TUBE AND ACCESSORIES received FDA 510(k) clearance on 2013-06-26, under 510(k) number K122653.

Who is the listed applicant for MIC-KEY SF LOW PROFILE GASTROSTOMY TUBE AND ACCESSORIES?

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

What is the FDA product code for MIC-KEY SF LOW PROFILE GASTROSTOMY TUBE AND ACCESSORIES?

The FDA product code for MIC-KEY SF LOW PROFILE GASTROSTOMY TUBE AND ACCESSORIES is KNT.

Related Clinical Trials

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.

Other records listing Kimberly-Clark Corporation as applicant

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.

View all 11 devices →

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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