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FDA 510(k)

CAREFREE(TM) FESTIVA PANTYSHIELDS

K-Number: K901664 · 1990-06-22

Decision Date1990-06-22
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CAREFREE(TM) FESTIVA PANTYSHIELDS 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 1990-06-22 under 510(k) number K901664. 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 CAREFREE(TM) FESTIVA PANTYSHIELDS?

CAREFREE(TM) FESTIVA PANTYSHIELDS is a medical device that received FDA 510(k) clearance on 1990-06-22. The listed applicant is Personal Products Co.. The 510(k) number is K901664.

When did CAREFREE(TM) FESTIVA PANTYSHIELDS receive FDA 510(k) clearance?

CAREFREE(TM) FESTIVA PANTYSHIELDS received FDA 510(k) clearance on 1990-06-22, under 510(k) number K901664.

Who is the listed applicant for CAREFREE(TM) FESTIVA PANTYSHIELDS?

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 CAREFREE(TM) FESTIVA PANTYSHIELDS?

The FDA product code for CAREFREE(TM) FESTIVA PANTYSHIELDS 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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