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FDA 510(k)

REGULAR DEODORANT MAXITHINS PADS

K-Number: K832972 · 1983-11-28

ApplicantTampax, Inc.
Decision Date1983-11-28
Product CodeHHL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

REGULAR DEODORANT MAXITHINS PADS is the device name listed in this FDA 510(k) record. The listed applicant is Tampax, Inc.. It received FDA 510(k) clearance on 1983-11-28 under 510(k) number K832972. 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 REGULAR DEODORANT MAXITHINS PADS?

REGULAR DEODORANT MAXITHINS PADS is a medical device that received FDA 510(k) clearance on 1983-11-28. The listed applicant is Tampax, Inc.. The 510(k) number is K832972.

When did REGULAR DEODORANT MAXITHINS PADS receive FDA 510(k) clearance?

REGULAR DEODORANT MAXITHINS PADS received FDA 510(k) clearance on 1983-11-28, under 510(k) number K832972.

Who is the listed applicant for REGULAR DEODORANT MAXITHINS PADS?

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

What is the FDA product code for REGULAR DEODORANT MAXITHINS PADS?

The FDA product code for REGULAR DEODORANT MAXITHINS PADS 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 Tampax, 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 12 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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