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FDA 510(k)

NATRACARE MENSTRUAL PADS

K-Number: K940329 · 1994-04-13

ApplicantNatracare, LLC
Decision Date1994-04-13
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

NATRACARE MENSTRUAL PADS is the device name listed in this FDA 510(k) record. The listed applicant is Natracare, LLC. It received FDA 510(k) clearance on 1994-04-13 under 510(k) number K940329. 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 NATRACARE MENSTRUAL PADS?

NATRACARE MENSTRUAL PADS is a medical device that received FDA 510(k) clearance on 1994-04-13. The listed applicant is Natracare, LLC. The 510(k) number is K940329.

When did NATRACARE MENSTRUAL PADS receive FDA 510(k) clearance?

NATRACARE MENSTRUAL PADS received FDA 510(k) clearance on 1994-04-13, under 510(k) number K940329.

Who is the listed applicant for NATRACARE MENSTRUAL PADS?

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

What is the FDA product code for NATRACARE MENSTRUAL PADS?

The FDA product code for NATRACARE MENSTRUAL PADS 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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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

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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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