FEMTEX 100% COTTON DENTLE TOUCH TAMPONS
K-Number: K970232 · 1997-03-21
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Device Summary
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
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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