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FDA 510(k)

LAURIER OVERNIGHT SANITARY NAPKIN

K-Number: K852922 · 1985-08-26

ApplicantKao Corp.
Decision Date1985-08-26
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LAURIER OVERNIGHT SANITARY NAPKIN is the device name listed in this FDA 510(k) record. The listed applicant is Kao Corp.. It received FDA 510(k) clearance on 1985-08-26 under 510(k) number K852922. The device is classified under product code HHD. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAURIER OVERNIGHT SANITARY NAPKIN?

LAURIER OVERNIGHT SANITARY NAPKIN is a medical device that received FDA 510(k) clearance on 1985-08-26. The listed applicant is Kao Corp.. The 510(k) number is K852922.

When did LAURIER OVERNIGHT SANITARY NAPKIN receive FDA 510(k) clearance?

LAURIER OVERNIGHT SANITARY NAPKIN received FDA 510(k) clearance on 1985-08-26, under 510(k) number K852922.

Who is the listed applicant for LAURIER OVERNIGHT SANITARY NAPKIN?

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

What is the FDA product code for LAURIER OVERNIGHT SANITARY NAPKIN?

The FDA product code for LAURIER OVERNIGHT SANITARY NAPKIN is HHD.

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 Kao 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.

View all 9 devices →

Related Devices (Code: HHD)

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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