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FDA 510(k)

KIMBERLY-CLARK INTRODUCER KITS

K-Number: K080253 · 2008-02-26

ApplicantKimberly-Clark Corp.
Decision Date2008-02-26
Product CodeKGC
Advisory CommitteeGU
DecisionUnknown

Device Summary

KIMBERLY-CLARK INTRODUCER KITS 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 2008-02-26 under 510(k) number K080253. The device is classified under product code KGC. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the KIMBERLY-CLARK INTRODUCER KITS?

KIMBERLY-CLARK INTRODUCER KITS is a medical device that received FDA 510(k) clearance on 2008-02-26. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K080253.

When did KIMBERLY-CLARK INTRODUCER KITS receive FDA 510(k) clearance?

KIMBERLY-CLARK INTRODUCER KITS received FDA 510(k) clearance on 2008-02-26, under 510(k) number K080253.

Who is the listed applicant for KIMBERLY-CLARK INTRODUCER KITS?

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 INTRODUCER KITS?

The FDA product code for KIMBERLY-CLARK INTRODUCER KITS 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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