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FDA 510(k)

UNSCENTED ALWAYS PANTILINERS

K-Number: K852985 · 1985-08-29

Decision Date1985-08-29
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

UNSCENTED ALWAYS PANTILINERS 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 1985-08-29 under 510(k) number K852985. 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 ALWAYS PANTILINERS?

UNSCENTED ALWAYS PANTILINERS is a medical device that received FDA 510(k) clearance on 1985-08-29. The listed applicant is Procter & Gamble Mfg. Co.. The 510(k) number is K852985.

When did UNSCENTED ALWAYS PANTILINERS receive FDA 510(k) clearance?

UNSCENTED ALWAYS PANTILINERS received FDA 510(k) clearance on 1985-08-29, under 510(k) number K852985.

Who is the listed applicant for UNSCENTED ALWAYS PANTILINERS?

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 UNSCENTED ALWAYS PANTILINERS?

The FDA product code for UNSCENTED ALWAYS PANTILINERS 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.

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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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