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FDA 510(k)

FEMTEX 100% COTTON DENTLE TOUCH TAMPONS

K-Number: K970232 · 1997-03-21

Decision Date1997-03-21
Product CodeHEB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

FEMTEX 100% COTTON DENTLE TOUCH TAMPONS is the device name listed in this FDA 510(k) record. The listed applicant is Regu-Tech Assoc., Inc.. It received FDA 510(k) clearance on 1997-03-21 under 510(k) number K970232. 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 FEMTEX 100% COTTON DENTLE TOUCH TAMPONS?

FEMTEX 100% COTTON DENTLE TOUCH TAMPONS is a medical device that received FDA 510(k) clearance on 1997-03-21. The listed applicant is Regu-Tech Assoc., Inc.. The 510(k) number is K970232.

When did FEMTEX 100% COTTON DENTLE TOUCH TAMPONS receive FDA 510(k) clearance?

FEMTEX 100% COTTON DENTLE TOUCH TAMPONS received FDA 510(k) clearance on 1997-03-21, under 510(k) number K970232.

Who is the listed applicant for FEMTEX 100% COTTON DENTLE TOUCH TAMPONS?

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

What is the FDA product code for FEMTEX 100% COTTON DENTLE TOUCH TAMPONS?

The FDA product code for FEMTEX 100% COTTON DENTLE TOUCH 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 Regu-Tech Assoc., 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.

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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