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FDA 510(k)

KOTEX(R) SECUREHOLD SUPER CURVE/CURVED MAXI PADS

K-Number: K925250 · 1993-03-03

ApplicantKimberly-Clark Corp.
Decision Date1993-03-03
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

KOTEX(R) SECUREHOLD SUPER CURVE/CURVED 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 1993-03-03 under 510(k) number K925250. 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(R) SECUREHOLD SUPER CURVE/CURVED MAXI PADS?

KOTEX(R) SECUREHOLD SUPER CURVE/CURVED MAXI PADS is a medical device that received FDA 510(k) clearance on 1993-03-03. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K925250.

When did KOTEX(R) SECUREHOLD SUPER CURVE/CURVED MAXI PADS receive FDA 510(k) clearance?

KOTEX(R) SECUREHOLD SUPER CURVE/CURVED MAXI PADS received FDA 510(k) clearance on 1993-03-03, under 510(k) number K925250.

Who is the listed applicant for KOTEX(R) SECUREHOLD SUPER CURVE/CURVED 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(R) SECUREHOLD SUPER CURVE/CURVED MAXI PADS?

The FDA product code for KOTEX(R) SECUREHOLD SUPER CURVE/CURVED 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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