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FDA 510(k)

ROSTAM SCENTED AND UNSCENTED PLASTIC APPLICATOR TAMPONS

K-Number: K062001 · 2006-12-07

ApplicantRostam , Ltd.
Decision Date2006-12-07
Product CodeHEB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ROSTAM SCENTED AND UNSCENTED 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 2006-12-07 under 510(k) number K062001. 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 SCENTED AND UNSCENTED PLASTIC APPLICATOR TAMPONS?

ROSTAM SCENTED AND UNSCENTED PLASTIC APPLICATOR TAMPONS is a medical device that received FDA 510(k) clearance on 2006-12-07. The listed applicant is Rostam , Ltd.. The 510(k) number is K062001.

When did ROSTAM SCENTED AND UNSCENTED PLASTIC APPLICATOR TAMPONS receive FDA 510(k) clearance?

ROSTAM SCENTED AND UNSCENTED PLASTIC APPLICATOR TAMPONS received FDA 510(k) clearance on 2006-12-07, under 510(k) number K062001.

Who is the listed applicant for ROSTAM SCENTED AND UNSCENTED 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 SCENTED AND UNSCENTED PLASTIC APPLICATOR TAMPONS?

The FDA product code for ROSTAM SCENTED AND UNSCENTED 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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