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FDA 510(k)

SURE & NATURAL(TM) UNSCENTED MENSTRUAL PAD

K-Number: K895519 · 1989-11-29

Decision Date1989-11-29
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SURE & NATURAL(TM) UNSCENTED MENSTRUAL PAD 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 1989-11-29 under 510(k) number K895519. 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 SURE & NATURAL(TM) UNSCENTED MENSTRUAL PAD?

SURE & NATURAL(TM) UNSCENTED MENSTRUAL PAD is a medical device that received FDA 510(k) clearance on 1989-11-29. The listed applicant is Personal Products Co.. The 510(k) number is K895519.

When did SURE & NATURAL(TM) UNSCENTED MENSTRUAL PAD receive FDA 510(k) clearance?

SURE & NATURAL(TM) UNSCENTED MENSTRUAL PAD received FDA 510(k) clearance on 1989-11-29, under 510(k) number K895519.

Who is the listed applicant for SURE & NATURAL(TM) UNSCENTED MENSTRUAL PAD?

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 SURE & NATURAL(TM) UNSCENTED MENSTRUAL PAD?

The FDA product code for SURE & NATURAL(TM) UNSCENTED MENSTRUAL PAD 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.

Other records listing Personal Products Co. 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.

View all 45 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.

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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