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FDA 510(k)

PANTY-LINERS UNSCENTED

K-Number: K830145 · 1983-01-21

Decision Date1983-01-21
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PANTY-LINERS UNSCENTED is the device name listed in this FDA 510(k) record. The listed applicant is Procter & Gamble Mfg. Co.. It received FDA 510(k) clearance on 1983-01-21 under 510(k) number K830145. 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 PANTY-LINERS UNSCENTED?

PANTY-LINERS UNSCENTED is a medical device that received FDA 510(k) clearance on 1983-01-21. The listed applicant is Procter & Gamble Mfg. Co.. The 510(k) number is K830145.

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

PANTY-LINERS UNSCENTED received FDA 510(k) clearance on 1983-01-21, under 510(k) number K830145.

Who is the listed applicant for PANTY-LINERS UNSCENTED?

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

What is the FDA product code for PANTY-LINERS UNSCENTED?

The FDA product code for PANTY-LINERS UNSCENTED 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 Procter & Gamble Mfg. 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 72 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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