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FDA 510(k)

ALICIA MENSTRUAL CUP

K-Number: K070965 · 2008-03-05

ApplicantAlicia International Pty , Ltd.
Decision Date2008-03-05
Product CodeHHE
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ALICIA MENSTRUAL CUP is the device name listed in this FDA 510(k) record. The listed applicant is Alicia International Pty , Ltd.. It received FDA 510(k) clearance on 2008-03-05 under 510(k) number K070965. The device is classified under product code HHE. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALICIA MENSTRUAL CUP?

ALICIA MENSTRUAL CUP is a medical device that received FDA 510(k) clearance on 2008-03-05. The listed applicant is Alicia International Pty , Ltd.. The 510(k) number is K070965.

When did ALICIA MENSTRUAL CUP receive FDA 510(k) clearance?

ALICIA MENSTRUAL CUP received FDA 510(k) clearance on 2008-03-05, under 510(k) number K070965.

Who is the listed applicant for ALICIA MENSTRUAL CUP?

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

What is the FDA product code for ALICIA MENSTRUAL CUP?

The FDA product code for ALICIA MENSTRUAL CUP is HHE.

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Related Devices (Code: HHE)

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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.

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