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FDA 510(k)

LAURIER SANITARY NAPKIN

K-Number: K843318 · 1984-10-15

ApplicantKao Corp.
Decision Date1984-10-15
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LAURIER 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 1984-10-15 under 510(k) number K843318. 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 SANITARY NAPKIN?

LAURIER SANITARY NAPKIN is a medical device that received FDA 510(k) clearance on 1984-10-15. The listed applicant is Kao Corp.. The 510(k) number is K843318.

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

LAURIER SANITARY NAPKIN received FDA 510(k) clearance on 1984-10-15, under 510(k) number K843318.

Who is the listed applicant for LAURIER 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 SANITARY NAPKIN?

The FDA product code for LAURIER 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.

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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.

K893773LAURIER SANITARY NAPKINK882768LAURIER SANITARY NAPKINK872481LAURIER NIGHT SAFE EXTRA PROTECTION SANITARY NAP.K862269LAURIER SANTARY NAPKIN (MODIFICATION)K862271LAURIER SAFETY LONG SANITARY NAPKIN (MODIFICATION)K862270LAURIER OVERNIGHT SANITARY NAPKIN (MODIFICATION)

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.

K071827ALWAYS MENSTRUAL PADSProcter & Gamble, Inc.K012629ALWAYS DUETSProcter & Gamble Co.K003843ENVIVE MINIFORMSProcter & Gamble Co.K993870UNSCENTED INTERLABIAL MENSTRUAL PADProcter & Gamble Co.K980395GLADRAGS COTTON MENSTRUAL PADKeepers!, Inc.K953470FLUSHIES FLUSHABLE/BIODEGRADABLE MENSTRUAL PADS/NAPKINS (ULTRA THINS)Mediquip, Inc.

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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