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FDA 510(k)

ROSTAM LTD. FRAGRANCED OR UNFRAGRANCED NEW PLASTIC APPLICATOR TAMPONS

K-Number: K090071 · 2009-05-28

ApplicantRostam , Ltd.
Decision Date2009-05-28
Product CodeHEB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ROSTAM LTD. FRAGRANCED OR UNFRAGRANCED NEW 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 2009-05-28 under 510(k) number K090071. 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 ROSTAM LTD. FRAGRANCED OR UNFRAGRANCED NEW PLASTIC APPLICATOR TAMPONS?

ROSTAM LTD. FRAGRANCED OR UNFRAGRANCED NEW PLASTIC APPLICATOR TAMPONS is a medical device that received FDA 510(k) clearance on 2009-05-28. The listed applicant is Rostam , Ltd.. The 510(k) number is K090071.

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

ROSTAM LTD. FRAGRANCED OR UNFRAGRANCED NEW PLASTIC APPLICATOR TAMPONS received FDA 510(k) clearance on 2009-05-28, under 510(k) number K090071.

Who is the listed applicant for ROSTAM LTD. FRAGRANCED OR UNFRAGRANCED NEW 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 OR UNFRAGRANCED NEW PLASTIC APPLICATOR TAMPONS?

The FDA product code for ROSTAM LTD. FRAGRANCED OR UNFRAGRANCED NEW 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.

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: 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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