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FDA 510(k)

KOTEX MAXI PADS

K-Number: K850033 · 1985-03-01

ApplicantKimberly-Clark Corp.
Decision Date1985-03-01
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

KOTEX MAXI PADS 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 1985-03-01 under 510(k) number K850033. 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 KOTEX MAXI PADS?

KOTEX MAXI PADS is a medical device that received FDA 510(k) clearance on 1985-03-01. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K850033.

When did KOTEX MAXI PADS receive FDA 510(k) clearance?

KOTEX MAXI PADS received FDA 510(k) clearance on 1985-03-01, under 510(k) number K850033.

Who is the listed applicant for KOTEX MAXI PADS?

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 KOTEX MAXI PADS?

The FDA product code for KOTEX MAXI PADS is HHD.

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Other records listing Kimberly-Clark Corp. as applicant

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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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