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FDA 510(k)

TAMPAX TAMPONS

K-Number: K820174 · 1982-03-18

ApplicantTampax, Inc.
Decision Date1982-03-18
Product CodeHEB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TAMPAX TAMPONS is the device name listed in this FDA 510(k) record. The listed applicant is Tampax, Inc.. It received FDA 510(k) clearance on 1982-03-18 under 510(k) number K820174. The device is classified under product code HEB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAMPAX TAMPONS?

TAMPAX TAMPONS is a medical device that received FDA 510(k) clearance on 1982-03-18. The listed applicant is Tampax, Inc.. The 510(k) number is K820174.

When did TAMPAX TAMPONS receive FDA 510(k) clearance?

TAMPAX TAMPONS received FDA 510(k) clearance on 1982-03-18, under 510(k) number K820174.

Who is the listed applicant for TAMPAX TAMPONS?

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 TAMPAX TAMPONS?

The FDA product code for TAMPAX TAMPONS is HEB.

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.

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Related Devices (Code: HEB)

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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