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FDA 510(k)

MAXI-PADS, STAYFREE

K-Number: K770778 · 1977-05-20

ApplicantPersonal Products Co.
Decision Date1977-05-20
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MAXI-PADS, STAYFREE is the device name listed in this FDA 510(k) record. The listed applicant is Personal Products Co.. It received FDA 510(k) clearance on 1977-05-20 under 510(k) number K770778. 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 MAXI-PADS, STAYFREE?

MAXI-PADS, STAYFREE is a medical device that received FDA 510(k) clearance on 1977-05-20. The listed applicant is Personal Products Co.. The 510(k) number is K770778.

When did MAXI-PADS, STAYFREE receive FDA 510(k) clearance?

MAXI-PADS, STAYFREE received FDA 510(k) clearance on 1977-05-20, under 510(k) number K770778.

Who is the listed applicant for MAXI-PADS, STAYFREE?

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

What is the FDA product code for MAXI-PADS, STAYFREE?

The FDA product code for MAXI-PADS, STAYFREE is HHD.

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Other records listing Personal Products Co. 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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