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FDA 510(k)

UNSCENTED MENSTRUAL LINER

K-Number: K953488 · 1995-08-09

Decision Date1995-08-09
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

UNSCENTED MENSTRUAL LINER 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 1995-08-09 under 510(k) number K953488. 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 MENSTRUAL LINER?

UNSCENTED MENSTRUAL LINER is a medical device that received FDA 510(k) clearance on 1995-08-09. The listed applicant is Paragon Trade Brands, Inc.. The 510(k) number is K953488.

When did UNSCENTED MENSTRUAL LINER receive FDA 510(k) clearance?

UNSCENTED MENSTRUAL LINER received FDA 510(k) clearance on 1995-08-09, under 510(k) number K953488.

Who is the listed applicant for UNSCENTED MENSTRUAL LINER?

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 MENSTRUAL LINER?

The FDA product code for UNSCENTED MENSTRUAL LINER 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

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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