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FDA 510(k)

PADS, MINI, MAXI DEODORANT

K-Number: K782111 · 1979-01-08

Decision Date1979-01-08
Product CodeHHL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PADS, MINI, MAXI DEODORANT is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Playtex, Inc.. It received FDA 510(k) clearance on 1979-01-08 under 510(k) number K782111. 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 PADS, MINI, MAXI DEODORANT?

PADS, MINI, MAXI DEODORANT is a medical device that received FDA 510(k) clearance on 1979-01-08. The listed applicant is Intl. Playtex, Inc.. The 510(k) number is K782111.

When did PADS, MINI, MAXI DEODORANT receive FDA 510(k) clearance?

PADS, MINI, MAXI DEODORANT received FDA 510(k) clearance on 1979-01-08, under 510(k) number K782111.

Who is the listed applicant for PADS, MINI, MAXI DEODORANT?

The FDA 510(k) record lists Intl. Playtex, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PADS, MINI, MAXI DEODORANT?

The FDA product code for PADS, MINI, MAXI DEODORANT 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 Intl. Playtex, Inc. 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: 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

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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