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FDA 510(k)

THE DIVACUP MENSTRUAL SOLUTION

K-Number: K021356 · 2002-07-16

ApplicantDiva International, Inc.
Decision Date2002-07-16
Product CodeHHE
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

THE DIVACUP MENSTRUAL SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Diva International, Inc.. It received FDA 510(k) clearance on 2002-07-16 under 510(k) number K021356. 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 THE DIVACUP MENSTRUAL SOLUTION?

THE DIVACUP MENSTRUAL SOLUTION is a medical device that received FDA 510(k) clearance on 2002-07-16. The listed applicant is Diva International, Inc.. The 510(k) number is K021356.

When did THE DIVACUP MENSTRUAL SOLUTION receive FDA 510(k) clearance?

THE DIVACUP MENSTRUAL SOLUTION received FDA 510(k) clearance on 2002-07-16, under 510(k) number K021356.

Who is the listed applicant for THE DIVACUP MENSTRUAL SOLUTION?

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

What is the FDA product code for THE DIVACUP MENSTRUAL SOLUTION?

The FDA product code for THE DIVACUP MENSTRUAL SOLUTION is HHE.

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Related Devices (Code: HHE)

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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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