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FDA 510(k)

MEDLINE GASTROSTOMY TUBE

K-Number: K073718 · 2008-03-19

ApplicantMedline Industries, Inc.
Decision Date2008-03-19
Product CodeKGC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MEDLINE GASTROSTOMY TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 2008-03-19 under 510(k) number K073718. The device is classified under product code KGC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDLINE GASTROSTOMY TUBE?

MEDLINE GASTROSTOMY TUBE is a medical device that received FDA 510(k) clearance on 2008-03-19. The listed applicant is Medline Industries, Inc.. The 510(k) number is K073718.

When did MEDLINE GASTROSTOMY TUBE receive FDA 510(k) clearance?

MEDLINE GASTROSTOMY TUBE received FDA 510(k) clearance on 2008-03-19, under 510(k) number K073718.

Who is the listed applicant for MEDLINE GASTROSTOMY TUBE?

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

What is the FDA product code for MEDLINE GASTROSTOMY TUBE?

The FDA product code for MEDLINE GASTROSTOMY TUBE is KGC.

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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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