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FDA 510(k)

UNSCENTED MENSTRAL PAD WITH WINGS

K-Number: K953666 · 1995-09-27

Decision Date1995-09-27
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

UNSCENTED MENSTRAL PAD WITH WINGS is the device name listed in this FDA 510(k) record. The listed applicant is Paragon Trade Brands, Inc.. It received FDA 510(k) clearance on 1995-09-27 under 510(k) number K953666. 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 UNSCENTED MENSTRAL PAD WITH WINGS?

UNSCENTED MENSTRAL PAD WITH WINGS is a medical device that received FDA 510(k) clearance on 1995-09-27. The listed applicant is Paragon Trade Brands, Inc.. The 510(k) number is K953666.

When did UNSCENTED MENSTRAL PAD WITH WINGS receive FDA 510(k) clearance?

UNSCENTED MENSTRAL PAD WITH WINGS received FDA 510(k) clearance on 1995-09-27, under 510(k) number K953666.

Who is the listed applicant for UNSCENTED MENSTRAL PAD WITH WINGS?

The FDA 510(k) record lists Paragon Trade Brands, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNSCENTED MENSTRAL PAD WITH WINGS?

The FDA product code for UNSCENTED MENSTRAL PAD WITH WINGS 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 Paragon Trade Brands, Inc. 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 14 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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