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FDA 510(k)

KIMLON IMPERVIOUS STOCKINETTES

K-Number: K790972 · 1979-06-05

ApplicantKimberly-Clark Corp.
Decision Date1979-06-05
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KIMLON IMPERVIOUS STOCKINETTES 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 1979-06-05 under 510(k) number K790972. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KIMLON IMPERVIOUS STOCKINETTES?

KIMLON IMPERVIOUS STOCKINETTES is a medical device that received FDA 510(k) clearance on 1979-06-05. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K790972.

When did KIMLON IMPERVIOUS STOCKINETTES receive FDA 510(k) clearance?

KIMLON IMPERVIOUS STOCKINETTES received FDA 510(k) clearance on 1979-06-05, under 510(k) number K790972.

Who is the listed applicant for KIMLON IMPERVIOUS STOCKINETTES?

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 KIMLON IMPERVIOUS STOCKINETTES?

The FDA product code for KIMLON IMPERVIOUS STOCKINETTES is KKX.

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Other records listing Kimberly-Clark Corp. as applicant

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Related Devices (Code: KKX)

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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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