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FDA 510(k)

WATER WORKS DOUCHING DEVICE

K-Number: K080200 · 2008-07-10

ApplicantAbbott Research Group, Inc.
Decision Date2008-07-10
Product CodeHED
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

WATER WORKS DOUCHING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Research Group, Inc.. It received FDA 510(k) clearance on 2008-07-10 under 510(k) number K080200. 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 WATER WORKS DOUCHING DEVICE?

WATER WORKS DOUCHING DEVICE is a medical device that received FDA 510(k) clearance on 2008-07-10. The listed applicant is Abbott Research Group, Inc.. The 510(k) number is K080200.

When did WATER WORKS DOUCHING DEVICE receive FDA 510(k) clearance?

WATER WORKS DOUCHING DEVICE received FDA 510(k) clearance on 2008-07-10, under 510(k) number K080200.

Who is the listed applicant for WATER WORKS DOUCHING DEVICE?

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

What is the FDA product code for WATER WORKS DOUCHING DEVICE?

The FDA product code for WATER WORKS DOUCHING DEVICE is HED.

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Related Devices (Code: HED)

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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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