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FDA 510(k)

KIMBERLY-CLARK CHILD/PEDIATRIC FACE MASK

K-Number: K103150 · 2011-09-23

Decision Date2011-09-23
Product CodeOXZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KIMBERLY-CLARK CHILD/PEDIATRIC FACE MASK is the device name listed in this FDA 510(k) record. The listed applicant is Kimberly-Clark. It received FDA 510(k) clearance on 2011-09-23 under 510(k) number K103150. The device is classified under product code OXZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KIMBERLY-CLARK CHILD/PEDIATRIC FACE MASK?

KIMBERLY-CLARK CHILD/PEDIATRIC FACE MASK is a medical device that received FDA 510(k) clearance on 2011-09-23. The listed applicant is Kimberly-Clark. The 510(k) number is K103150.

When did KIMBERLY-CLARK CHILD/PEDIATRIC FACE MASK receive FDA 510(k) clearance?

KIMBERLY-CLARK CHILD/PEDIATRIC FACE MASK received FDA 510(k) clearance on 2011-09-23, under 510(k) number K103150.

Who is the listed applicant for KIMBERLY-CLARK CHILD/PEDIATRIC FACE MASK?

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

What is the FDA product code for KIMBERLY-CLARK CHILD/PEDIATRIC FACE MASK?

The FDA product code for KIMBERLY-CLARK CHILD/PEDIATRIC FACE MASK is OXZ.

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 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.

Related Devices (Code: OXZ)

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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