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FDA 510(k)

UNSCENTED PANTY SHIELDS

K-Number: K830224 · 1983-02-08

Decision Date1983-02-08
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

UNSCENTED PANTY SHIELDS is the device name listed in this FDA 510(k) record. The listed applicant is Weyerhaeuser Co.. It received FDA 510(k) clearance on 1983-02-08 under 510(k) number K830224. 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 PANTY SHIELDS?

UNSCENTED PANTY SHIELDS is a medical device that received FDA 510(k) clearance on 1983-02-08. The listed applicant is Weyerhaeuser Co.. The 510(k) number is K830224.

When did UNSCENTED PANTY SHIELDS receive FDA 510(k) clearance?

UNSCENTED PANTY SHIELDS received FDA 510(k) clearance on 1983-02-08, under 510(k) number K830224.

Who is the listed applicant for UNSCENTED PANTY SHIELDS?

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

What is the FDA product code for UNSCENTED PANTY SHIELDS?

The FDA product code for UNSCENTED PANTY SHIELDS 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 Weyerhaeuser 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 10 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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