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FDA 510(k)

ATHENA PELVIC MUSCLE TRAINER II

K-Number: K033256 · 2003-12-30

Decision Date2003-12-30
Product CodeKPI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ATHENA PELVIC MUSCLE TRAINER II is the device name listed in this FDA 510(k) record. The listed applicant is Athena Feminine Technologies, Inc.. It received FDA 510(k) clearance on 2003-12-30 under 510(k) number K033256. The device is classified under product code KPI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATHENA PELVIC MUSCLE TRAINER II?

ATHENA PELVIC MUSCLE TRAINER II is a medical device that received FDA 510(k) clearance on 2003-12-30. The listed applicant is Athena Feminine Technologies, Inc.. The 510(k) number is K033256.

When did ATHENA PELVIC MUSCLE TRAINER II receive FDA 510(k) clearance?

ATHENA PELVIC MUSCLE TRAINER II received FDA 510(k) clearance on 2003-12-30, under 510(k) number K033256.

Who is the listed applicant for ATHENA PELVIC MUSCLE TRAINER II?

The FDA 510(k) record lists Athena Feminine Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ATHENA PELVIC MUSCLE TRAINER II?

The FDA product code for ATHENA PELVIC MUSCLE TRAINER II is KPI.

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 Athena Feminine Technologies, Inc. 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.

Related Devices (Code: KPI)

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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