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)

ROSTAM LTD FRAGRANCED PLASTIC APPLICATOR TAMPONS

K-Number: K032080 · 2003-08-14

ApplicantRostam , Ltd.
Decision Date2003-08-14
Product CodeHIL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ROSTAM LTD FRAGRANCED 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 2003-08-14 under 510(k) number K032080. The device is classified under product code HIL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROSTAM LTD FRAGRANCED PLASTIC APPLICATOR TAMPONS?

ROSTAM LTD FRAGRANCED PLASTIC APPLICATOR TAMPONS is a medical device that received FDA 510(k) clearance on 2003-08-14. The listed applicant is Rostam , Ltd.. The 510(k) number is K032080.

When did ROSTAM LTD FRAGRANCED PLASTIC APPLICATOR TAMPONS receive FDA 510(k) clearance?

ROSTAM LTD FRAGRANCED PLASTIC APPLICATOR TAMPONS received FDA 510(k) clearance on 2003-08-14, under 510(k) number K032080.

Who is the listed applicant for ROSTAM LTD FRAGRANCED 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 ROSTAM LTD FRAGRANCED PLASTIC APPLICATOR TAMPONS?

The FDA product code for ROSTAM LTD FRAGRANCED PLASTIC APPLICATOR TAMPONS is HIL.

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 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.

View all 9 devices →

Related Devices (Code: HIL)

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.

↑