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FDA 510(k)

WORRY-REMOVER IRRIGATOR

K-Number: K030056 · 2003-04-22

ApplicantCorisen Group, Ltd.
Decision Date2003-04-22
Product CodeHED
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

WORRY-REMOVER IRRIGATOR is the device name listed in this FDA 510(k) record. The listed applicant is Corisen Group, Ltd.. It received FDA 510(k) clearance on 2003-04-22 under 510(k) number K030056. The device is classified under product code HED. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WORRY-REMOVER IRRIGATOR?

WORRY-REMOVER IRRIGATOR is a medical device that received FDA 510(k) clearance on 2003-04-22. The listed applicant is Corisen Group, Ltd.. The 510(k) number is K030056.

When did WORRY-REMOVER IRRIGATOR receive FDA 510(k) clearance?

WORRY-REMOVER IRRIGATOR received FDA 510(k) clearance on 2003-04-22, under 510(k) number K030056.

Who is the listed applicant for WORRY-REMOVER IRRIGATOR?

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

What is the FDA product code for WORRY-REMOVER IRRIGATOR?

The FDA product code for WORRY-REMOVER IRRIGATOR is HED.

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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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