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FDA 510(k)

SCENTED ALWAYS PANTILINERS

K-Number: K853000 · 1985-09-06

Decision Date1985-09-06
Product CodeHHL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SCENTED 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 1985-09-06 under 510(k) number K853000. The device is classified under product code HHL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCENTED ALWAYS PANTILINERS?

SCENTED ALWAYS PANTILINERS is a medical device that received FDA 510(k) clearance on 1985-09-06. The listed applicant is Procter & Gamble Mfg. Co.. The 510(k) number is K853000.

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

SCENTED ALWAYS PANTILINERS received FDA 510(k) clearance on 1985-09-06, under 510(k) number K853000.

Who is the listed applicant for SCENTED 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 SCENTED ALWAYS PANTILINERS?

The FDA product code for SCENTED ALWAYS PANTILINERS is HHL.

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: HHL)

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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