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FDA 510(k)

ASSURE DEODORANT TAMPONS

K-Number: K771012 · 1977-06-24

Decision Date1977-06-24
Product CodeHIL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ASSURE DEODORANT TAMPONS 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 1977-06-24 under 510(k) number K771012. The device is classified under product code HIL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASSURE DEODORANT TAMPONS?

ASSURE DEODORANT TAMPONS is a medical device that received FDA 510(k) clearance on 1977-06-24. The listed applicant is Personal Products Co.. The 510(k) number is K771012.

When did ASSURE DEODORANT TAMPONS receive FDA 510(k) clearance?

ASSURE DEODORANT TAMPONS received FDA 510(k) clearance on 1977-06-24, under 510(k) number K771012.

Who is the listed applicant for ASSURE DEODORANT TAMPONS?

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 ASSURE DEODORANT TAMPONS?

The FDA product code for ASSURE DEODORANT TAMPONS is HIL.

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: HIL)

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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