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FDA 510(k)

STERILITE STERILIZATION KIT

K-Number: K864596 · 1986-12-18

ApplicantKimberly-Clark Corp.
Decision Date1986-12-18
Product Code
DecisionSubstantially Equivalent

Device Summary

STERILITE STERILIZATION KIT 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 1986-12-18 under 510(k) number K864596. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILITE STERILIZATION KIT?

STERILITE STERILIZATION KIT is a medical device that received FDA 510(k) clearance on 1986-12-18. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K864596.

When did STERILITE STERILIZATION KIT receive FDA 510(k) clearance?

STERILITE STERILIZATION KIT received FDA 510(k) clearance on 1986-12-18, under 510(k) number K864596.

Who is the listed applicant for STERILITE STERILIZATION KIT?

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

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Other records listing Kimberly-Clark Corp. 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.

K131879KC 300 SURGICAL MASKK131841KIMBERLY-CLARK LAVENDER NITRILE POWDER-FREE EXAM GLOVEK131254KIMVENT MICROCUFF SUBGLOTTIC SUCTIONING ENDOTRACHEAL TUBEK120985KIMVENT MICROCUFF SUBGLOTTIC SUCTIONINGK112805KIMGUARD ONE-STEP STERILIZATION WRAPK113423KIMBERLY CLARK PURPLE NITRILE, AND PURPLE NITRILE XTRA POWDER FREE EXAM GLOVE

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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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