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)

INTERLUDE AND OTHER PRIVATE LABEL PLASTIC APPLICATOR TAMPONS

K-Number: K020535 · 2002-05-09

ApplicantRostam , Ltd.
Decision Date2002-05-09
Product CodeHEB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

INTERLUDE AND OTHER PRIVATE LABEL PLASTIC APPLICATOR TAMPONS is the device name listed in this FDA 510(k) record. The listed applicant is Rostam , Ltd.. It received FDA 510(k) clearance on 2002-05-09 under 510(k) number K020535. 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 INTERLUDE AND OTHER PRIVATE LABEL PLASTIC APPLICATOR TAMPONS?

INTERLUDE AND OTHER PRIVATE LABEL PLASTIC APPLICATOR TAMPONS is a medical device that received FDA 510(k) clearance on 2002-05-09. The listed applicant is Rostam , Ltd.. The 510(k) number is K020535.

When did INTERLUDE AND OTHER PRIVATE LABEL PLASTIC APPLICATOR TAMPONS receive FDA 510(k) clearance?

INTERLUDE AND OTHER PRIVATE LABEL PLASTIC APPLICATOR TAMPONS received FDA 510(k) clearance on 2002-05-09, under 510(k) number K020535.

Who is the listed applicant for INTERLUDE AND OTHER PRIVATE LABEL PLASTIC APPLICATOR TAMPONS?

The FDA 510(k) record lists Rostam , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTERLUDE AND OTHER PRIVATE LABEL PLASTIC APPLICATOR TAMPONS?

The FDA product code for INTERLUDE AND OTHER PRIVATE LABEL PLASTIC APPLICATOR 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.

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 Rostam , Ltd. 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.

K102445ROSTAM SCENTED AND UNSCENTED BIODEGRADABLE PLASTIC APPLICATOR TAMPONSK090071ROSTAM LTD. FRAGRANCED OR UNFRAGRANCED NEW PLASTIC APPLICATOR TAMPONSK062001ROSTAM SCENTED AND UNSCENTED PLASTIC APPLICATOR TAMPONSK042773ROSTAM SCENTED AND UNSCENTED PLASTIC APPLICATOR TAMPONSK030474PH BUFFERING PLASTIC APPLICATOR TAMPONK032080ROSTAM LTD FRAGRANCED PLASTIC APPLICATOR TAMPONS

View all 9 devices →

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.

↑