TAMPAX(R) L PLASTIC TAMPONS, UNSCENTED
K-Number: K131543 · 2013-06-20
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Device Summary
Frequently Asked Questions
What is the TAMPAX(R) L PLASTIC TAMPONS, UNSCENTED?
TAMPAX(R) L PLASTIC TAMPONS, UNSCENTED is a medical device that received FDA 510(k) clearance on 2013-06-20. The listed applicant is Procter & Gamble Co.. The 510(k) number is K131543.
When did TAMPAX(R) L PLASTIC TAMPONS, UNSCENTED receive FDA 510(k) clearance?
TAMPAX(R) L PLASTIC TAMPONS, UNSCENTED received FDA 510(k) clearance on 2013-06-20, under 510(k) number K131543.
Who is the listed applicant for TAMPAX(R) L PLASTIC TAMPONS, UNSCENTED?
The FDA 510(k) record lists Procter & Gamble Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TAMPAX(R) L PLASTIC TAMPONS, UNSCENTED?
The FDA product code for TAMPAX(R) L PLASTIC TAMPONS, UNSCENTED 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 Procter & Gamble Co. 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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