Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

TAMPAX C PLASTIC TAMPONS, UNSCENTED

K-Number: K110669 · 2011-06-02

ApplicantThe Procter & Gamble Co.
Decision Date2011-06-02
Product CodeHEB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TAMPAX C PLASTIC TAMPONS, UNSCENTED is the device name listed in this FDA 510(k) record. The listed applicant is The Procter & Gamble Co.. It received FDA 510(k) clearance on 2011-06-02 under 510(k) number K110669. 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 C PLASTIC TAMPONS, UNSCENTED?

TAMPAX C PLASTIC TAMPONS, UNSCENTED is a medical device that received FDA 510(k) clearance on 2011-06-02. The listed applicant is The Procter & Gamble Co.. The 510(k) number is K110669.

When did TAMPAX C PLASTIC TAMPONS, UNSCENTED receive FDA 510(k) clearance?

TAMPAX C PLASTIC TAMPONS, UNSCENTED received FDA 510(k) clearance on 2011-06-02, under 510(k) number K110669.

Who is the listed applicant for TAMPAX C PLASTIC TAMPONS, UNSCENTED?

The FDA 510(k) record lists The Procter & Gamble Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TAMPAX C PLASTIC TAMPONS, UNSCENTED?

The FDA product code for TAMPAX C 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing The 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.

K091419VICKS POWERSHOT DRY THROAT & MOUTH RELIEF

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.

K252005Livi DeviceLiviwell, Inc.K253719Unscented Menstrual Long Applicator Tampon; Unscented Menstrual Cardboard Applicator Tampon; Unscented Menstrual Digital TamponsUnibeauty (Hubei) Technology Co., Ltd.K252939COHITECH ORGANIC COTTON COMPACT APPLICATOR TAMPONSCotton High Tech S.L.K252613Unscented menstrual three-piece applicator tamponUnibeauty (Hubei) Technology Co., Ltd.K251033Unscented menstrual long applicator tampon; Unscented menstrual Compact Applicator Tampon; Unscented menstrual Cardboard Applicator Tampon; Unscented menstrual Digital TamponsUnibeauty (Hubei) Technology Co., Ltd.K242105SABA TamponsEssity Higiene Y Salud Mexico. S.A. DE C.V.

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.

↑